Motivational interviewing for substance use reduction
Open accessAbstract
BACKGROUND: Substance use is a global issue, with around 30 to 35 million individuals estimated to have a substance-use disorder. Motivational interviewing (MI) is a client-centred method that aims to strengthen a person's motivation and commitment to a specific goal by exploring their reasons for change and resolving ambivalence, in an atmosphere of acceptance and compassion. This review updates the 2011 version by Smedslund and colleagues. OBJECTIVES: To assess the effectiveness of motivational interviewing for substance use on the extent of substance use, readiness to change, and retention in treatment. SEARCH METHODS: We searched 18 electronic databases, six websites, four mailing lists, and the reference lists of included studies and reviews. The last search dates were in February 2021 and November 2022. SELECTION CRITERIA: We included randomised controlled trials with individuals using drugs, alcohol, or both. Interventions were MI or motivational enhancement therapy (MET), delivered individually and face to face. Eligible control interventions were no intervention, treatment as usual, assessment and feedback, or other active intervention. DATA COLLECTION AND ANALYSIS: We used standard methodological procedures expected by Cochrane, and assessed the certainty of evidence with GRADE. We conducted meta-analyses for the three outcomes (extent of substance use, readiness to change, retention in treatment) at four time points (post-intervention, short-, medium-, and long-term follow-up). MAIN RESULTS: = 75%; 6 studies, 471 participants; low-certainty evidence). The effect was weaker at short-term follow-up (SMD 0.20, 95% CI 0.12 to 0.28; 19 studies, 3351 participants; very low-certainty evidence). This comparison revealed a difference in favour of MI at medium-term follow-up (SMD 0.12, 95% CI 0.05 to 0.20; 16 studies, 3137 participants; low-certainty evidence) and no difference at long-term follow-up (SMD 0.12, 95% CI -0.00 to 0.25; 9 studies, 1525 participants; very low-certainty evidence). There was no difference in readiness to change (SMD 0.05, 95% CI -0.11 to 0.22; 5 studies, 1495 participants; very low-certainty evidence). Retention in treatment was slightly higher with MI (SMD 0.26, 95% CI -0.00 to 0.52; 2 studies, 427 participants; very low-certainty evidence). Comparing MI to treatment as usual revealed a very small negative effect in substance use post-intervention (SMD -0.14, 95% CI -0.27 to -0.02; 5 studies, 976 participants; very low-certainty evidence). There was no difference at short-term follow-up (SMD 0.07, 95% CI -0.03 to 0.17; 14 studies, 3066 participants), a very small benefit of MI at medium-term follow-up (SMD 0.12, 95% CI 0.02 to 0.22; 9 studies, 1624 participants), and no difference at long-term follow-up (SMD 0.06, 95% CI -0.05 to 0.17; 8 studies, 1449 participants), all with low-certainty evidence. There was no difference in readiness to change (SMD 0.06, 95% CI -0.27 to 0.39; 2 studies, 150 participants) and retention in treatment (SMD -0.09, 95% CI -0.34 to 0.16; 5 studies, 1295 participants), both with very low-certainty evidence. Comparing MI to assessment and feedback revealed no difference in substance use at short-term follow-up (SMD 0.09, 95% CI -0.05 to 0.23; 7 studies, 854 participants; low-certainty evidence). A small benefit for MI was shown at medium-term (SMD 0.24, 95% CI 0.08 to 0.40; 6 studies, 688 participants) and long-term follow-up (SMD 0.24, 95% CI 0.07 to 0.41; 3 studies, 448 participants), both with moderate-certainty evidence. None of the studies in this comparison measured substance use at the post-intervention time point, readiness to change, and retention in treatment. Comparing MI to another active intervention revealed no difference in substance use at any follow-up time point, all with low-certainty evidence: post-intervention (SMD 0.07, 95% CI -0.15 to 0.29; 3 studies, 338 participants); short-term (SMD 0.05, 95% CI -0.03 to 0.13; 18 studies, 2795 participants); medium-term (SMD 0.08, 95% CI -0.01 to 0.17; 15 studies, 2352 participants); and long-term follow-up (SMD 0.03, 95% CI -0.07 to 0.13; 10 studies, 1908 participants). There was no difference in readiness to change (SMD 0.15, 95% CI -0.00 to 0.30; 5 studies, 988 participants; low-certainty evidence) and retention in treatment (SMD -0.04, 95% CI -0.23 to 0.14; 12 studies, 1945 participants; moderate-certainty evidence). We downgraded the certainty of evidence due to inconsistency, study limitations, publication bias, and imprecision. AUTHORS' CONCLUSIONS: Motivational interviewing may reduce substance use compared with no intervention up to a short follow-up period. MI probably reduces substance use slightly compared with assessment and feedback over medium- and long-term periods. MI may make little to no difference to substance use compared to treatment as usual and another active intervention. It is unclear if MI has an effect on readiness to change and retention in treatment. The studies in
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8 of 29 cited sources checked · 3 supported · 1 flagged · accuracy not yet measured
- Premisecitation
At least 18 systematic reviews and meta-analyses of motivational interviewing have been published since 2000.
“At least 18 systematic reviews and meta-analyses of motivational interviewing have been published since 2000 (Andréasson 2003;Burke 2003;Burke 2004;Carey 2007;de Wildt 2002;Dunn 2001;Emmelkamp 2006;Grenard 2006;Hettema 2005;Larimer 2007;Lundahl 2010;Macdonald 2012;Magill 2018;Mbuagbaw 2012;Nahom 2005;Rubak 2005;Vasilaki 2006;Zomahoun 2017).”
Quote in the paperSubstantial claim1 of 3 sources checked - Premisecitation
Lindson 2019 showed no benefit of motivational interviewing compared with other interventions over medium- and long-term follow-up of over six months.
“It showed no benefit of motivational interviewing compared with other interventions over medium-and long-term follow-up of over six months.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites Lindson 2019 source
The Discussion (page unavailable) reports that neither reduction-to-quit nor abrupt-quitting interventions produced superior long-term quit rates. The Results identify motivational interviewing as an arm of one included trial, but the review does not establish the claimed general finding that motivational interviewing had no benefit compared with other interventions over follow-up exceeding six months. (LLM, conf=0.82)
Experimental — accuracy not yet measured
- Findingown data
There was only one study in which the participants were explicitly described as having mental problems (Martino 2006).
“There was only one study in which the participants were explicitly described as having mental problems (Martino 2006)”
Quote in the paperSubstantial claim1 of 1 sources checked- cites Martino 2006 source
- Findingnone given
It is unclear whether motivational interviewing has an effect on staying in treatment.
“It is unclear whether motivational interviewing has an effect on willingness to change and staying in treatment.”
Quote in the paperSubstantial claim - Findingown data
18 of the included studies involved fewer than 100 people.
“The results were very inconsistent across the different studies, and 18 of the studies involved fewer than 100 people.”
Quote in the paperSubstantial claim
- Findingnone given
The results were very inconsistent across the different studies.
“The results were very inconsistent across the different studies, and 18 of the studies involved fewer than 100 people.”
Quote in the paperSubstantial claim - Findingown data
Motivational interviewing may make little to no difference to substance use compared with another active intervention.
“The results show that motivational interviewing may make little to no difference to substance use compared with regular treatment or another active intervention.”
Quote in the paperSubstantial claim - Findingown data
In the short term, motivational interviewing may reduce substance use compared with no treatment.
“However, in the short term, motivational interviewing may reduce substance use compared with no treatment.”
Quote in the paperSubstantial claim - Findingown data
At medium- and long-term follow-up, motivational interviewing probably reduces substance use slightly compared with assessment and feedback.
“At medium-and long-term follow-up, motivational interviewing probably reduces substance use slightly compared with assessment and feedback.”
Quote in the paperSubstantial claim - Findingown data
The review found 93 studies involving 22,776 people with substance use.
“We found 93 studies that involved 22,776 people with substance use.”
Quote in the paperNot a substantial claim - Findingreasoning
The review has moderate to no confidence in the evidence because of concerns about how some of the studies were conducted.
“We have moderate to no confidence in the evidence because of concerns about how some of the studies were conducted.”
Quote in the paperSubstantial claim - Findingnone given
It is unclear whether motivational interviewing has an effect on willingness to change.
“It is unclear whether motivational interviewing has an effect on willingness to change and staying in treatment.”
Quote in the paperNot a substantial claim - Findingown data
Motivational interviewing may make little to no difference to substance use compared with regular treatment.
“The results show that motivational interviewing may make little to no difference to substance use compared with regular treatment or another active intervention.”
Quote in the paperSubstantial claim - Findingown data
For motivational interviewing versus no intervention at short-term follow-up, pooling 19 studies with 3351 participants revealed a small benefit for motivational interviewing (SMD 0.20, 95% CI 0.12 to 0.28; I2 = 27%; very low-certainty evidence).
“Short-term follow-up: pooling 19 studies with 3351 participants revealed a small benefit for motivational interviewing (SMD 0.20, 95% CI 0.12 to 0.28; I 2 = 27%; very low-certainty evidence; Analysis 1.1.2).”
Quote in the paperSubstantial claim - Findingown data
For motivational interviewing versus no intervention at medium-term follow-up, pooling 16 studies with 3137 participants revealed a difference in favour of motivational interviewing (SMD 0.12, 95% CI 0.05 to 0.20; I2 = 5%; low-certainty evidence).
“Medium-term follow-up: pooling 16 studies with 3137 participants revealed a difference in favour of motivational interviewing (SMD 0.12, 95% CI 0.05 to 0.20; I 2 = 5%; low-certainty evidence; Analysis 1.1.3).”
Quote in the paperSubstantial claim - Findingown data
A subgroup analysis of five studies (440 participants) on alcohol use revealed a benefit for motivational interviewing comparable to the original analysis (SMD 0.44, 95% CI -0.00 to 0.89; I2 = 79%).
“A subgroup analysis of five studies (440 participants) on alcohol use revealed a benefit for motivational interviewing comparable to the original analysis (SMD 0.44, 95% CI -0.00 to 0.89; I 2 = 79%).”
Quote in the paperNot a substantial claim - Findingown data
For motivational interviewing versus no intervention at long-term follow-up, pooling nine studies with 1525 participants revealed no difference between groups (SMD 0.12, 95% CI -0.00 to 0.25; I2 = 22%; very low-certainty evidence).
“Long-term follow-up: pooling nine studies with 1525 participants revealed no difference between groups (SMD 0.12, 95% CI -0.00 to 0.25; I 2 = 22%; very low-certainty evidence; Analysis 1.1.4).”
Quote in the paperSubstantial claim - Findingown data
A subgroup analysis of five studies with 395 participants who received more than one motivational interviewing session revealed a slightly lower benefit for motivational interviewing (SMD 0.37, 95% CI -0.05 to 0.79; I2 = 69%).
“A second subgroup analysis of five studies with 395 participants who received more than one motivational interviewing session revealed a slightly lower benefit for motivational interviewing (SMD 0.37, 95% CI -0.05 to 0.79) with substantial heterogeneity (I 2 = 69%).”
Quote in the paperNot a substantial claim - Findingown data
For the motivational interviewing versus no intervention comparison, smaller studies tend to have larger effect sizes in favour of motivational interviewing.
“For the motivational interviewing versus no intervention comparison, it appears that smaller studies tend to have larger effect sizes in favour of motivational interviewing.”
Quote in the paperNot a substantial claim - Findingown data
For motivational interviewing versus another active intervention, retention in treatment: pooling twelve studies with 1945 participants revealed no difference (SMD -0.04, 95% CI -0.23 to 0.14; I2 = 48%; moderate-certainty evidence).
“Pooling twelve studies with 1945 participants revealed no difference between motivational interviewing and another active intervention (SMD -0.04, 95% CI -0.23 to 0.14; I 2 = 48%; moderatecertainty evidence; Analysis 4.3).”
Quote in the paperSubstantial claim - Findingown data
For motivational interviewing versus treatment as usual, readiness to change: pooling two studies with 150 participants revealed no difference (SMD 0.06, 95% CI -0.27 to 0.39; I2 = 0%; very low-certainty evidence).
“Pooling two studies with 150 participants revealed no difference between motivational interviewing and treatment as usual (SMD 0.06, 95% CI -0.27 to 0.39; I 2 = 0%; very low-certainty evidence; Analysis 2.2).”
Quote in the paperNot a substantial claim - Findingown data
The evidence for motivational interviewing versus no intervention was downgraded due to inconsistency, serious or very serious study limitations, publication bias, or imprecision.
“We downgraded the evidence due to inconsistency, serious or very serious study limitations, publication bias, or imprecision.”
Quote in the paperSubstantial claim - Findingown data
For motivational interviewing versus assessment and feedback at short-term follow-up, pooling seven studies with 854 participants revealed no difference (SMD 0.09, 95% CI -0.05 to 0.23; I2 = 0%; low-certainty evidence).
“Short-term follow-up: pooling seven studies with 854 participants revealed no difference between motivational interviewing and assessment and feedback (SMD 0.09, 95% CI -0.05 to 0.23; I 2 = 0%; low-certainty evidence; Analysis 3.1.1).”
Quote in the paperSubstantial claim - Findingown data
Subgroup analyses revealed a difference between groups for type of substance (P = 0.0005) between users of more than one drug versus users of alcohol.
“Subgroup analyses revealed differences between groups for: (a) type of substance (P = 0.0005) between the studies with users of more than one drug versus users of alcohol”
Quote in the paperSubstantial claim - Findingown data
A subgroup analysis of 10 studies with 2496 participants who used more than one substance showed no benefit of motivational interviewing compared with treatment as usual (SMD 0.00, 95% CI -0.07 to 0.08; I2 = 0%).
“A subgroup analysis of 10 studies with 2496 participants who used more than one substance showed no benefit of motivational interviewing compared with treatment as usual (SMD 0.00, 95% CI -0.07 to 0.08; I 2 = 0%).”
Quote in the paperSubstantial claim - Findingown data
For motivational interviewing versus treatment as usual, retention in treatment: pooling five studies with 1295 participants revealed no benefit for motivational interviewing (SMD -0.09, 95% CI -0.34 to 0.16; I2 = 0%; very low-certainty evidence).
“Six studies reported on retention in treatment, but we were only able to calculate an effect size for five studies with 1295 participants, which revealed no benefit for motivational interviewing (SMD -0.09, 95% CI -0.34 to 0.16; I 2 = 0%; very lowcertainty evidence; Analysis 2.3).”
Quote in the paperSubstantial claim - Findingown data
Subgroup analyses revealed a difference between groups for intensity of the intervention (P = 0.02).
“and (b) intensity of the intervention (P = 0.02)”
Quote in the paperSubstantial claim - Findingown data
A subgroup analysis of three studies with 698 participants showed a small benefit of motivational interviewing on alcohol use (SMD 0.33, 95% CI 0.16 to 0.50; I2 = 0%).
“A subgroup analysis of three studies with 698 participants showed a small benefit of motivational interviewing on alcohol use (SMD 0.33, 95% CI 0.16 to 0.50; I 2 = 0%).”
Quote in the paperSubstantial claim - Findingown data
For motivational interviewing versus another active intervention at medium-term follow-up, pooling 15 studies with 2352 participants revealed no difference (SMD 0.08, 95% CI -0.01 to 0.17; I2 = 13%).
“Medium-term follow-up: pooling 15 studies with 2352 participants revealed no difference between the two treatments (SMD 0.08, 95% CI -0.01 to 0.17; I 2 = 13%).”
Quote in the paperSubstantial claim - Findingcitation
Another study did not show reductions in binge-drinking or concurrent substance use over 12 or 15 months (Stein 2017), based on data from 161 and 160 participants, respectively.
“Another study did not show reductions in bingedrinking or concurrent substance use over 12 or 15 months (Stein 2017), based on data from 161 and 160 participants, respectively”
Quote in the paperNot a substantial claim - Findingown data
Sensitivity analyses removing studies with high or unclear risk of bias revealed no difference in treatment effects.
“Our sensitivity analyses to assess the robustness of the results revealed no difference in the treatment effects when we removed studies with high or unclear risk of bias from the analysis.”
Quote in the paperSubstantial claim - Findingown data
For motivational interviewing versus another active intervention at short-term follow-up, pooling 18 studies with 2795 participants revealed no difference (SMD 0.05, 95% CI -0.03 to 0.13; I2 = 0%).
“Short-term follow-up: pooling 18 studies with 2795 participants revealed no difference between motivational interviewing and another active intervention (SMD 0.05, 95% CI -0.03 to 0.13; I 2 = 0%).”
Quote in the paperSubstantial claim - Findingown data
For motivational interviewing versus no intervention, readiness to change: pooling five studies with 1495 participants revealed no difference (SMD 0.05, 95% CI -0.11 to 0.22; I2 = 48%; very low-certainty evidence).
“Pooling five studies with 1495 participants revealed no difference between motivational interviewing and no intervention (SMD 0.05, 95% CI -0.11 to 0.22; I 2 = 48%; very low-certainty evidence; Analysis 1.2).”
Quote in the paperNot a substantial claim - Findingnone given
Smaller studies with larger effect sizes were reported at short- and medium-term follow-up.
“We also reported smaller studies with larger effect sizes at short-and medium-term follow-up.”
Quote in the paperNot a substantial claim - Findingown data
For motivational interviewing versus treatment as usual at long-term follow-up, pooling eight studies with 1449 participants found no differences (SMD 0.06, 95% CI -0.05 to 0.17; I2 = 0%; low-certainty evidence).
“Long-term follow-up: pooling eight studies with 1449 participants found no differences between groups (SMD of 0.06, 95% CI -0.05 to 0.17; I 2 = 0%; low-certainty evidence; Analysis 2.1.4).”
Quote in the paperSubstantial claim - Findingown data
For motivational interviewing versus treatment as usual at short-term follow-up, pooling 14 studies with 3066 participants revealed no difference (SMD 0.07, 95% CI -0.03 to 0.17; I2 = 44%; low-certainty evidence).
“Short-term follow-up: pooling 14 studies with 3066 participants revealed no difference between the two groups (SMD 0.07, 95% CI -0.03 to 0.17; I 2 = 44%; low-certainty evidence; Analysis 2.1.2).”
Quote in the paperSubstantial claim - Findingreasoning
For the motivational interviewing versus no intervention comparison, the certainty of evidence was judged to be low or very low.
“For the motivational interviewing versus no intervention comparison, we judged the certainty of evidence to be low or very low.”
Quote in the paperSubstantial claim - Findingown data
There was comparable retention in treatment for motivational interviewing versus other active intervention (SMD -0.04, 95% CI -0.23 to 0.14), with moderate-certainty evidence.
“There was comparable retention in treatment for the motivational interviewing versus other active intervention comparison (SMD -0.04, 95% CI -0.23 to 0.14), with moderate-certainty evidence.”
Quote in the paperSubstantial claim - Findingown data
For motivational interviewing versus treatment as usual at post-intervention, pooling five studies with 976 participants revealed a very small negative effect of motivational interviewing (SMD -0.14, 95% CI -0.27 to -0.02; I2 = 0%; very low-certainty evidence).
“Post-intervention: pooling five studies with 976 participants revealed a very small negative effect of motivational interviewing (SMD -0.14, 95% CI -0.27 to -0.02;I 2 = 0%; very low-certainty evidence; Analysis 2.1.1).”
Quote in the paperSubstantial claim - Findingown data
For motivational interviewing versus treatment as usual at medium-term follow-up, pooling nine studies with 1624 participants revealed a very small benefit of motivational interviewing (SMD 0.12, 95% CI 0.02 to 0.22; I2 = 0%; low-certainty evidence).
“Medium-term follow-up: pooling nine studies with 1624 participants revealed a very small benefit of motivational interviewing (SMD 0.12, 95% CI 0.02 to 0.22; I 2 = 0%; low-certainty evidence; Analysis 2.1.3).”
Quote in the paperSubstantial claim - Findingcitation
The third study reported no change in binge-drinking or concurrent use of alcohol and cannabis after six and nine months (Stein 2017), based on data from 173 and 162 participants, respectively.
“The third study reported no change in binge-drinking or concurrent use of alcohol and cannabis a er six and nine months (Stein 2017), based on data from 173 and 162 participants, respectively”
Quote in the paperNot a substantial claim - Findingown data
Two of three additional studies reported a reduction in primary drug or alcohol use at six months (Aharonovich 2017; Logan 2015).
“Two of three additional studies reported a reduction in primary drug or alcohol use at six months (Aharonovich 2017; Logan 2015).”
Quote in the paperNot a substantial claim - Findingown data
Subgroup analyses revealed no difference between groups for age group, comparing adults to adolescents/young adults (P = 0.36).
“but not for (c) age group, comparing adults to adolescents/ young adults (P = 0.36).”
Quote in the paperNot a substantial claim - Findingown data
For motivational interviewing versus another active intervention at long-term follow-up, pooling ten studies with 1908 participants revealed no difference (SMD 0.03, 95% CI -0.07 to 0.13; I2 = 11%).
“Long-term follow-up: pooling ten studies with 1908 participants revealed no difference between treatments (SMD 0.03, 95% CI -0.07 to 0.13; I 2 = 11%).”
Quote in the paperSubstantial claim - Findingown data
For motivational interviewing versus assessment and feedback at long-term follow-up, three studies with 448 participants showed a small benefit of motivational interviewing (SMD 0.24, 95% CI 0.07 to 0.41; I2 = 0%; moderate-certainty evidence).
“Long-term follow-up: three studies with 448 participants showed a small benefit of motivational interviewing (SMD 0.24, 95% CI 0.07 to 0.41; I 2 = 0%; moderate-certainty evidence; Analysis 3.1.3).”
Quote in the paperSubstantial claim - Findingnone given
The certainty of evidence was judged as low or very low for most of the remaining comparisons and outcomes.
“We judged the certainty of evidence as low or very low for most of the remaining comparisons and outcomes.”
Quote in the paperSubstantial claim - Findingcitation
A small study with 74 participants stated no benefit of motivational interviewing on cannabis use (D'Amico 2008).
“A small study with 74 participants stated no benefit of motivational interviewing on cannabis use (D'Amico 2008).”
Quote in the paperNot a substantial claim - Findingown data
For motivational interviewing versus assessment and feedback at medium-term follow-up, pooling six studies with 688 participants revealed a small benefit for motivational interviewing (SMD 0.24, 95% CI 0.08 to 0.40; I2 = 0%; moderate-certainty evidence).
“Medium-term follow-up: pooling six studies with 688 participants revealed a small benefit for motivational interviewing (SMD 0.24, 95% CI 0.08 to 0.40; I 2 = 0%; moderate-certainty evidence; Analysis”
Quote in the paperSubstantial claim - Findingcitation
Another study reported no change in binge-drinking or concurrent use of alcohol and cannabis at one and three months (Stein 2017), based on data from 195 and 178 participants, respectively.
“Another study reported no change in binge-drinking or concurrent use of alcohol and cannabis at one and three months (Stein 2017), based on data from 195 and 178 participants, respectively”
Quote in the paperNot a substantial claim - Findingown data
For motivational interviewing versus another active intervention at post-intervention, pooling three studies with 338 participants revealed no difference (SMD 0.07, 95% CI -0.15 to 0.29; I2 = 0%; low-certainty evidence).
“Post-intervention: pooling three studies with 338 participants revealed no difference between motivational interviewing and another active intervention (SMD 0.07, 95% CI -0.15 to 0.29; I 2 = 0%; low-certainty evidence; Analysis 4.1).”
Quote in the paperSubstantial claim - Findingown data
For motivational interviewing versus no intervention, retention in treatment: meta-analysis of two studies with 427 participants revealed no difference (SMD 0.26, 95% CI -0.0 to 0.52; I2 = 36%; very low-certainty evidence).
“Meta-analysis revealed no difference between motivational interviewing and no intervention (SMD 0.26, 95% CI -0.0 to 0.52; I 2 = 36%; very low-certainty evidence).”
Quote in the paperSubstantial claim - Findingown data
A subgroup analysis of six studies with 1337 participants and more than one session showed no benefit of motivational interviewing (SMD -0.05, 95% CI -0.16 to 0.05).
“A subgroup analysis of six studies with 1337 participants and more than one session showed no benefit of motivational interviewing (SMD -0.05, 95% CI -0.16 to 0.05).”
Quote in the paperNot a substantial claim - Findingown data
A subgroup analysis of eight studies with 1921 participants and a single intervention session of motivational interviewing lasting 15 to 120 minutes showed a very small benefit of motivational interviewing compared with treatment as usual (SMD 0.14, 95% CI 0.02 to 0.27; I2 = 37%).
“A subgroup analysis of eight studies with 1921 participants and a single intervention session of motivational interviewing lasting 15 to 120 minutes showed a very small benefit of motivational interviewing compared with treatment as usual (SMD 0.14, 95% CI 0.02 to 0.27; I 2 = 37%).”
Quote in the paperNot a substantial claim - Findingreasoning
The certainty of evidence for a small benefit of motivational interviewing compared to assessment and feedback (SMD 0.24, 95% CI 0.08 to 0.40) was moderate.
“We judged the certainty of evidence for a small benefit of motivational interviewing compared to assessment and feedback (SMD 0.24, 95% CI 0.08 to 0.40) as moderate”
Quote in the paperSubstantial claim - Findingown data
For motivational interviewing versus another active intervention, readiness to change: pooling five studies with 988 participants revealed no difference (SMD 0.15, 95% CI -0.00 to 0.30; I2 = 19%; low-certainty evidence).
“Pooling five studies with 988 participants revealed no difference in readiness to change between motivational interviewing and another active intervention (SMD 0.15, 95% CI -0.00 to 0.30; I 2 = 19%; Analysis 4.2).”
Quote in the paperNot a substantial claim - Findingnone given
The main areas of heterogeneity were different study populations, duration and frequency of the intervention, outcome measurement, and study quality.
“The main areas of heterogeneity were different study populations, duration and frequency of the intervention, outcome measurement, and study quality.”
Quote in the paperSubstantial claim - Findingcitation
One additional study reported a reduction in the use of non-injectable drugs at 12 months (RR 0.54, 95% CI 0.31 to 0.94; Aharonovich 2017), based on data from 137 participants.
“One additional study reported a reduction in the use of non-injectable drugs (RR 0.54, 95% CI 0.31 to 0.94) at 12 months (Aharonovich 2017), based on data from 137 participants”
Quote in the paperNot a substantial claim - Findingreasoning
Because of inconsistent reporting of quality conditions across studies, it was not possible to report overall fidelity of intervention implementation.
“Because of inconsistent reporting of quality conditions across studies, it was not possible to report overall fidelity of intervention implementation.”
Quote in the paperSubstantial claim - Findingown data
Results from randomised controlled trials have shown that motivational interviewing may reduce drug and alcohol use compared with no or minimal intervention.
“Nevertheless, results from randomised controlled trials have shown that motivational interviewing may reduce drug and alcohol use compared with no or minimal intervention.”
Quote in the paperSubstantial claim - Findingown data
Based on evidence of 93 randomised controlled trials with 22,776 participants, this review indicates that motivational interviewing may reduce substance use compared to no intervention for a short period of time.
“Based on the evidence of 93 randomised controlled trials with 22,776 participants, this review indicates that motivational interviewing may reduce substance use compared to no intervention for a short period of time”
Quote in the paperSubstantial claim - Findingown data
Motivational interviewing probably reduces substance use slightly compared to assessment and feedback at medium- and long-term follow-up.
“and probably reduces substance use slightly compared to assessment and feedback at medium-and long-term follow-up.”
Quote in the paperSubstantial claim - Findingreasoning
When motivational interviewing is compared with other psychosocial interventions, it has been found to be neither superior nor inferior.
“When motivational interviewing is compared with other psychosocial interventions, it has been found to be neither superior nor inferior”
Quote in the paperSubstantial claim - Findingown data
In the comparison of motivational interviewing versus no intervention, the overall effect on extent of substance use at post-intervention was statistically significant (Z = 2.27, P = 0.02).
“Test for overall effect: Z = 2.27 (P = 0.02)”
Quote in the paperSubstantial claim - Findingown data
In the comparison of motivational interviewing versus other active intervention, the medium-term follow-up analysis of extent of substance use showed low heterogeneity (Tau2 = 0.00; Chi2 = 16.05, df = 14, P = 0.31; I2 = 13%).
“Heterogeneity: Tau² = 0.00; Chi² = 16.05,df = 14 (P = 0.31); I² = 13%”
Quote in the paperNot a substantial claim - Findingown data
In the comparison of motivational interviewing versus treatment as usual, the medium-term follow-up analysis of extent of substance use showed no heterogeneity (Tau2 = 0.00; Chi2 = 7.47, df = 8, P = 0.49; I2 = 0%).
“Heterogeneity: Tau² = 0.00; Chi² = 7.47, df = 8 (P = 0.49); I² = 0%”
Quote in the paperNot a substantial claim - Findingown data
In the comparison of motivational interviewing versus no intervention, the post-intervention analysis of extent of substance use showed substantial heterogeneity (Tau2 = 0.18; Chi2 = 19.85, df = 5, P = 0.001; I2 = 75%).
“Heterogeneity: Tau² = 0.18; Chi² = 19.85,df = 5 (P = 0.001); I² = 75%”
Quote in the paperNot a substantial claim - Findingown data
In the comparison of motivational interviewing versus other active intervention, the overall effect on extent of substance use at short-term follow-up was not statistically significant (Z = 1.26, P = 0.21).
“Test for overall effect: Z = 1.26 (P = 0.21)”
Quote in the paperSubstantial claim - Findingown data
In the comparison of motivational interviewing versus no intervention, the short-term follow-up analysis of extent of substance use showed moderate heterogeneity (Tau2 = 0.01; Chi2 = 24.50, df = 18, P = 0.14; I2 = 27%).
“Heterogeneity: Tau² = 0.01; Chi² = 24.50,df = 18 (P = 0.14); I² = 27%”
Quote in the paperNot a substantial claim - Findingown data
In the comparison of motivational interviewing versus no intervention, the overall effect on extent of substance use at medium-term follow-up was statistically significant (Z = 3.13, P = 0.002).
“Test for overall effect: Z = 3.13 (P = 0.002)”
Quote in the paperSubstantial claim - Findingown data
In the comparison of motivational interviewing versus treatment as usual, the post-intervention analysis of extent of substance use showed no heterogeneity (Tau2 = 0.00; Chi2 = 3.90, df = 4, P = 0.42; I2 = 0%).
“Heterogeneity: Tau² = 0.00; Chi² = 3.90, df = 4 (P = 0.42); I² = 0%”
Quote in the paperNot a substantial claim - Findingown data
In the comparison of motivational interviewing versus no intervention, the overall effect on extent of substance use at short-term follow-up was statistically significant (Z = 5.04, P < 0.00001).
“Test for overall effect: Z = 5.04 (P < 0.00001)”
Quote in the paperSubstantial claim - Findingown data
In the comparison of motivational interviewing versus other active intervention, the overall effect on extent of substance use at post-intervention was not statistically significant (Z = 0.62, P = 0.53).
“Test for overall effect: Z = 0.62 (P = 0.53)”
Quote in the paperSubstantial claim - Findingown data
In the comparison of motivational interviewing versus other active intervention, the overall effect on extent of substance use at long-term follow-up was not statistically significant (Z = 0.52, P = 0.60).
“Test for overall effect: Z = 0.52 (P = 0.60)”
Quote in the paperSubstantial claim - Findingown data
In the comparison of motivational interviewing versus other active intervention, retention in treatment showed no statistically significant difference (SMD -0.04, 95% CI -0.23 to 0.14).
“4.3 Retention in treatment 12 1945 Std.Mean Difference (IV, Random, 95% CI) -0.04 [-0.23, 0.14]”
Quote in the paperNot a substantial claim - Findingown data
In the comparison of motivational interviewing versus treatment as usual, the overall effect on extent of substance use at short-term follow-up was not statistically significant (Z = 1.33, P = 0.18).
“Test for overall effect: Z = 1.33 (P = 0.18)”
Quote in the paperNot a substantial claim - Findingown data
In the comparison of motivational interviewing versus other active intervention, the short-term follow-up analysis of extent of substance use showed no heterogeneity (Tau2 = 0.00; Chi2 = 12.95, df = 17, P = 0.74; I2 = 0%).
“Heterogeneity: Tau² = 0.00; Chi² = 12.95, df = 17 (P = 0.74); I² = 0%”
Quote in the paperNot a substantial claim - Findingown data
In the comparison of motivational interviewing versus no intervention, the medium-term follow-up analysis of extent of substance use showed low heterogeneity (Tau2 = 0.00; Chi2 = 15.75, df = 15, P = 0.40; I2 = 5%).
“Heterogeneity: Tau² = 0.00; Chi² = 15.75, df = 15 (P = 0.40); I² = 5%”
Quote in the paperNot a substantial claim - Findingown data
In the comparison of motivational interviewing versus other active intervention, the post-intervention analysis of extent of substance use showed no heterogeneity (Tau2 = 0.00; Chi2 = 1.88, df = 2, P = 0.39; I2 = 0%).
“Heterogeneity: Tau² = 0.00; Chi² = 1.88, df = 2 (P = 0.39); I² = 0%”
Quote in the paperNot a substantial claim - Findingown data
In the comparison of motivational interviewing versus treatment as usual, the long-term follow-up analysis of extent of substance use showed no heterogeneity (Tau2 = 0.00; Chi2 = 4.80, df = 7, P = 0.68; I2 = 0%).
“Heterogeneity: Tau² = 0.00; Chi² = 4.80, df = 7 (P = 0.68); I² = 0%”
Quote in the paperNot a substantial claim - Findingown data
In the comparison of motivational interviewing versus treatment as usual, the overall effect on extent of substance use at medium-term follow-up was statistically significant (Z = 2.39, P = 0.02).
“Test for overall effect: Z = 2.39 (P = 0.02)”
Quote in the paperSubstantial claim - Findingown data
In the comparison of motivational interviewing versus treatment as usual, the overall effect on extent of substance use at long-term follow-up was not statistically significant (Z = 1.10, P = 0.27).
“Test for overall effect: Z = 1.10 (P = 0.27)”
Quote in the paperSubstantial claim - Findingown data
In the comparison of motivational interviewing versus treatment as usual, the overall effect on extent of substance use at post-intervention was statistically significant (Z = 2.21, P = 0.03).
“Test for overall effect: Z = 2.21 (P = 0.03)”
Quote in the paperSubstantial claim - Findingown data
In the comparison of motivational interviewing versus treatment as usual, the short-term follow-up analysis of extent of substance use showed moderate heterogeneity (Tau2 = 0.01; Chi2 = 23.15, df = 13, P = 0.04; I2 = 44%).
“Heterogeneity: Tau² = 0.01; Chi² = 23.15,df = 13 (P = 0.04); I² = 44%”
Quote in the paperNot a substantial claim - Findingown data
In the comparison of motivational interviewing versus other active intervention, the long-term follow-up analysis of extent of substance use showed low heterogeneity (Tau2 = 0.00; Chi2 = 10.11, df = 9, P = 0.34; I2 = 11%).
“Heterogeneity: Tau² = 0.00; Chi² = 10.11,df = 9 (P = 0.34); I² = 11%”
Quote in the paperNot a substantial claim - Findingown data
In the comparison of motivational interviewing versus other active intervention, the overall effect on extent of substance use at medium-term follow-up was not statistically significant (Z = 1.80, P = 0.07).
“Test for overall effect: Z = 1.80 (P = 0.07)”
Quote in the paperSubstantial claim - Premisenone given
Other previous reviews included randomised trials and other study designs.
“Other reviews have included randomised trials and other study designs.”
Quote in the paperSubstantial claim - Study design and conductown data
Forty-six studies were judged low risk for incomplete outcome data.
“We judged 46 studies as low risk because they adequately accounted for incomplete outcome data.”
Quote in the paperNot a substantial claim - Study design and conductreasoning
Fifty-nine studies were considered low risk for selective reporting.
“For most studies (n = 59), we considered the risk of selective reporting as low”
Quote in the paperNot a substantial claim - Study design and conductown data
Sixty-six studies inadequately described allocation concealment and were rated unclear risk.
“Most studies inadequately described what, if anything, was done to conceal the allocation (n = 66); we therefore rated these as having an unclear risk of bias.”
Quote in the paperNot a substantial claim - Study design and conductown data
Thirteen studies were classified as high risk for selective reporting.
“and as high for 13 studies”
Quote in the paperNot a substantial claim - Study design and conductown data
Twenty-five studies reported adequate details to ensure adequate allocation concealment.
“Twenty-five studies reported adequate details (e.g.central allocation via a secure web-based system; on-site computer with a locked file that could only be accessed a er entering participant data; stratified block randomisation using random allocation so ware by the study statistician) to ensure adequate allocation concealment.”
Quote in the paperNot a substantial claim - Study design and conductown data
With a two-sided alpha of 0.01 and power of 0.95, a total sample size of 1786 was necessary to detect a small standardised mean difference (SMD = 0.2).
“With a two-sided alpha of 0.01 and power of 0.95, we calculated that a total sample size of 1786 was necessary to detect a small standardised mean difference (SMD = 0.2).”
Quote in the paperSubstantial claim - Study design and conductown data
In 58 of the 93 studies, risk of performance and detection bias was rated high for participants, providers, or both.
“In 58 of the 93 studies, we rated the risk of performance and detection bias as high for participants, providers, or both”
Quote in the paperNot a substantial claim - Study design and conductown data
The remaining 24 studies were not at high risk of bias in any domains.
“We deemed that the remaining 24 studies were not at high risk of bias in any domains”
Quote in the paperNot a substantial claim - Study design and conductown data
Fifteen studies were classified as high risk for other potential sources of bias.
“and 15 studies as high risk for other potential sources of bias”
Quote in the paperNot a substantial claim - Study design and conductown data
Overall, 69 studies were judged to be at high risk of bias in at least one domain.
“Overall, we judged 69 studies to be at high risk of bias in at least one domain.”
Quote in the paperNot a substantial claim - Study design and conductown data
The certainty of the evidence was downgraded by one additional level due to attrition bias in studies whose total weight exceeded 50% in the meta-analysis.
“and downgraded by one additional level due to attrition bias in studies whose total weight exceeded 50% in the meta-analysis.”
Quote in the paperSubstantial claim - Interpretationreasoning
Lack of blinding could potentially have led to a risk of performance or detection bias.
“The lack of blinding could potentially have led to a risk of performance or detection bias.”
Quote in the paperSubstantial claim - Study design and conductown data
Publication bias may play a role because 41 studies, mostly conference abstracts, were classified as awaiting classification as no final publication with results could be found.
“However, publication bias may play a role in the sense that we classified 41 studies, mostly conference abstracts, as awaiting classification as we could not find a final publication with results.”
Quote in the paperNot a substantial claim - Study design and conductown data
Evidence certainty was downgraded due to inconsistency, with moderate to substantial heterogeneity between study results for the motivational interviewing versus no intervention comparison.
“We also downgraded evidence certainty due to inconsistency, with moderate to substantial heterogeneity between study results for the motivational interviewing versus no intervention comparison”
Quote in the paperSubstantial claim - Interpretationown data
The moderate heterogeneity in treatment effects when comparing motivational interviewing and treatment as usual at short-term follow-up could be explained by the higher benefit in studies of alcohol use compared to studies where more than one substance was used or where only a single intervention session was given.
“The moderate heterogeneity in treatment effects when comparing motivational interviewing and treatment as usual at short-term follow-up could be explained by the higher benefit in studies of alcohol use compared to studies where more than one substance was used or where only a single intervention session of motivational interviewing was given.”
Quote in the paperSubstantial claim - Study design and conductown data
Interpretation of funnel plots resulted in a downgrade due to publication bias for the motivational interviewing versus no intervention comparison.
“Interpretation of funnel plots (Figure 4; Figure 5; Figure 6; Figure 7) resulted in a downgrade due to publication bias for this same”
Quote in the paperSubstantial claim - Interpretationown data
Compared to treatment as usual or any other active intervention, there was no benefit of motivational interviewing in terms of extent of substance use at any time during follow-up.
“Compared to treatment as usual or any other active intervention, there was no benefit of motivational interviewing in terms of extent of substance use at any time during follow-up.”
Quote in the paperSubstantial claim - Study design and conductreasoning
The moderate certainty for motivational interviewing versus assessment and feedback was downgraded due to serious study limitations with unclear reporting or other risk of bias in most studies.
“downgrading due to serious study limitations with unclear reporting or other risk of bias in most studies.”
Quote in the paperSubstantial claim - Study design and conductown data
The certainty of the evidence was downgraded by one level due to unclear or high risk of bias in the randomisation procedure in most studies or for other risks of bias.
“We downgraded the certainty of the evidence by one level due to unclear or high risk of bias in the randomisation procedure in most studies or for other risks of bias”
Quote in the paperSubstantial claim - Premisereasoning
Due to the nature of the intervention, blinding of interventionists and participants is not possible.
“Due to the nature of the intervention, blinding of the interventionists and participants is not possible.”
Quote in the paperSubstantial claim - Interpretationown data
The results revealed no effect of motivational interviewing on the outcomes of readiness to change and retention in treatment.
“Our results revealed no effect of motivational interviewing on the outcomes of readiness to change and retention in treatment.”
Quote in the paperSubstantial claim - Interpretationreasoning
The downgrading of evidence was due to limitations in study design.
“The downgrading of evidence was due to limitations in study design.”
Quote in the paperSubstantial claim - Study design and conductown data
In Bell 2007, random sequence generation was at high risk of selection bias because allocation was semi-random.
“Random sequence generation (selection bias) High risk Semi-randomly allocated (”
Quote in the paperNot a substantial claim - Study design and conductown data
In Bernstein 2009, allocation concealment was at low risk because a double opaque envelope system blinded research assistants.
“Allocation concealment (selection bias) Low risk”
Quote in the paperNot a substantial claim - Study design and conductown data
In Bell 2007, allocation concealment was at high risk of selection bias because allocation was semi-random.
“Allocation concealment (selection bias) High risk Semi-randomly allocated (”
Quote in the paperNot a substantial claim - Study design and conductown data
In Bell 2007, selective reporting was at high risk because not all planned outcomes were reported.
“Selective reporting (reporting bias) High risk Not all of planned outcomes have been reported.”
Quote in the paperNot a substantial claim - Study design and conductown data
In Bernstein 2009, blinding of assessors was at low risk because participants were cautioned not to reveal testing.
“Blinding (performance bias and detection bias) Assessors Low risk”
Quote in the paperNot a substantial claim - Study design and conductreasoning
In Carey 2011, blinding of assessors was at high risk because outcomes were self-reported.
“Blinding (performance bias and detection bias) Assessors High risk Self-reported outcomes.”
Quote in the paperNot a substantial claim - Study design and conductreasoning
In Borsari 2012, blinding of assessors was at high risk because self-reported web-based questionnaires on drug use were used without physiological control.
“Blinding (performance bias and detection bias) Assessors High risk Self-reported results in web-based questionnaires on drug use without physiological control.”
Quote in the paperNot a substantial claim - Study design and conductown data
In Brown 2015, selective reporting was at high risk because no results for long-term follow-up were reported.
“Selective reporting (reporting bias) High risk No results for long-term follow-up reported.”
Quote in the paperNot a substantial claim - Study design and conductown data
For Kay-Lambkin 2009, blinding of patients and providers was at high risk of bias.
“Blinding (performance bias and detection bias) Patients and providers High risk No blinding.”
Quote in the paperNot a substantial claim - Study design and conductown data
For Kay-Lambkin 2009, incomplete outcome data was at high risk of bias.
“Incomplete outcome data (attrition bias) All outcomes High risk 28% attrition at 1 month, 31% attrition at 6 months, and 38% attrition at 12 months' follow-up.”
Quote in the paperNot a substantial claim - Study design and conductown data
For Logan 2015, incomplete outcome data was at high risk of bias.
“Incomplete outcome data (attrition bias) All outcomes High risk Follow-up of 82.4%, 75.0%, and 76.5% at 3, 6, and 12 months, respectively.”
Quote in the paperNot a substantial claim - Study design and conductown data
For Marijuana Treatment Project 2004, incomplete outcome data was at low risk of bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk Loss to follow-up at 4 months, 9 months, and 15 months were 11%, 13%, and 17%, respectively.Balanced.No reasons for loss reported.ITT performed (analysis of missing cases using baseline values.)”
Quote in the paperNot a substantial claim - Study design and conductreasoning
For Kelly 2000, blinding of assessors was at high risk of bias.
“Blinding (performance bias and detection bias) Assessors High risk Physiological measurement of blood alcohol content and urine samples provided immediate screen to ensure that participants were not intoxicated at the time of MRI data collection, but did not serve as a control for self-reported substance use.”
Quote in the paperNot a substantial claim - Study design and conductown data
For Kelly 2000, incomplete outcome data was at high risk of bias.
“Incomplete outcome data (attrition bias) All outcomes High risk Follow-up of 82.4%, 75.0%, and 76.5% at 3, 6, and 12 months, respectively.”
Quote in the paperNot a substantial claim - Study design and conductown data
For Mertens 2014, incomplete outcome data was at low risk of bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk 90% follow-up at 3 months with small differences between groups.”
Quote in the paperNot a substantial claim - Study design and conductown data
For Mertens 2014, blinding of patients and providers was at high risk of bias.
“Blinding (performance bias and detection bias) High risk Single-blinded trial (only research interviewers were blinded to randomisation status).”
Quote in the paperNot a substantial claim - Study design and conductown data
For McCambridge 2008, incomplete outcome data was at low risk of bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk 17% and 19% lost to follow-up at 3 and 6 months, respectively.Unequal between groups.Reasons for loss to follow-up not stated.ITT analysis using last observation carried forward.”
Quote in the paperNot a substantial claim - Study design and conductreasoning
For MATCH 1993, blinding of patients and providers was at low risk of bias.
“Blinding (performance bias and detection bias) Patients and providers Low risk No blinding, but most outcomes were physiological, also used to validate selfreports, and not likely to be influenced by lack of blinding.”
Quote in the paperNot a substantial claim - Study design and conductown data
For Marsden 2006, incomplete outcome data was at low risk of bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk 13% attrition at 6-month follow-up, balanced across conditions.Reasons not provided.”
Quote in the paperNot a substantial claim - Study design and conductown data
For Mastroleo 2010, blinding of patients and providers was at high risk of bias.
“Blinding (performance bias and detection bias) Patients and providers High risk Participants and providers were not blinded to treatment allocation.”
Quote in the paperNot a substantial claim - Study design and conductown data
For Mertens 2014, selective reporting was at high risk of bias.
“Selective reporting (reporting bias) High risk For the pre-planned outcome readiness to change, only baseline data are presented.”
Quote in the paperNot a substantial claim - Study design and conductown data
For MATCH 1993, incomplete outcome data was at low risk of bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk Attrition was less than 10% at 3, 6, 9, 12, and 15 months' follow-up in the after-care and outpatient groups.Balanced.Reasons for 3-year attrition in the outpatient group given.”
Quote in the paperNot a substantial claim - Study design and conductown data
In Logan 2015, blinding of outcome assessors was at high risk of bias because only self-reported outcomes were used.
“Blinding (performance bias and detection bias) Assessors High risk Only self-reported outcomes.”
Quote in the paperNot a substantial claim - Study design and conductown data
In Logan 2015, selective reporting was at high risk of bias because not all outcome data from the different follow-up points were reported.
“Selective reporting (reporting bias) High risk Not all outcome data from the different follow-up points were reported.”
Quote in the paperNot a substantial claim - Study design and conductreasoning
In Logan 2015, blinding of patients and providers was at high risk of bias because only the BASIC sessions were individual, so blinding was not possible.
“Blinding (performance bias and detection bias) Patients and providers High risk Only BASIC sessions were individual, blinding not possible.”
Quote in the paperNot a substantial claim - Study design and conductown data
In Logan 2015, incomplete outcome data was at high risk of bias: 57% completed all three follow-up assessments, 21% completed some follow-up, and 21% did not complete any follow-up.
“Incomplete outcome data (attrition bias) All outcomes High risk 57% completed all three follow-up assessments, 21% completed some follow-up, and 21% did not complete any follow-up.”
Quote in the paperNot a substantial claim - Study design and conductown data
In the included study assessed, blinding of outcome assessors was at high risk of bias because only self-reported outcomes were available.
“Blinding (performance bias and detection bias) Assessors High risk Only self-reported outcomes available.”
Quote in the paperNot a substantial claim
- Classified as probably not a substantial claim. 396
- May combine two claims. 207
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationThe Lindson 2019 review on motivational interviewing for smoking cessation included 12 trials and 4157 participants.
“The Lindson 2019 review on motivational interviewing for smoking cessation included 12 trials and 4157 participants.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites Lindson 2019 source
The paper’s Main results report 51 trials with 22,509 participants, not 12 trials with 4,157 participants. Its Discussion identifies the review’s focus as smoking reduction before quitting, not motivational interviewing. (LLM, conf=0.95)
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measured
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationAs in our review, most studies in Lindson 2019 reported that motivational interviewing techniques were used but did not describe the content in detail.
“As in our review, the authors note that most studies reported that motivational interviewing techniques were used but did not describe the content in detail.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites Lindson 2019 source
The Discussion (page unavailable) says studies typically gave only limited explanations of intervention content. The Results identify motivational interviewing in Cook 2016, but the passages do not say that most included studies used motivational interviewing techniques. The claim applies the review’s general observation about limited detail specifically to motivational interviewing in most studies, which the cited passages do not establish. (LLM, conf=0.84)
Experimental — accuracy not yet measured
May combine two claims.
InterpretationcitationThe effects of the intervention may have been overestimated because participants were not blinded and substance use was self-reported.
“There is also the possibility that the effects of the intervention were overestimated because participants were not blinded (Hrobjartsson 2014), and substance use was self-reported.”
Quote in the paperSubstantial claim1 of 1 sources checked- cites Hrobjartsson 2014 source
- Rests on an assumption: Substance use outcomes in the included studies were self-reported.
May combine two claims.
PremisecitationThe Klimas 2018 review examined several psychosocial interventions for alcohol use, including motivational interviewing, and found no difference between interventions.
“The Klimas 2018 review examined several psychosocial interventions for alcohol use, including motivational interviewing, and found no difference between interventions.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites Klimas 2018 source
The Discussion (Summary of main results) says the review assessed eight psychosocial interventions, including motivational interviewing, and found no significant alcohol-use differences in most comparisons. But it reports an exception: brief motivational interviewing was associated with a greater reduction in drinking days than assessment-only. The Key results also note a possible benefit of intensive over standard motivational interviewing among women, so the unqualified claim of no difference between interventions overstates the findings. (LLM, conf=0.89)
Experimental — accuracy not yet measured
May combine two claims.
Premisenone givenKlimas 2018 included only two studies, which used different scales to assess alcohol use.
“However, Klimas 2018 included only two studies, which used different scales to assess alcohol use.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites Klimas 2018 source
The Included studies section says the 2018 review included seven studies, not two. The Selective reporting section says the included studies used different questionnaires to measure their outcomes, supporting the point about differing measures. Page numbers were not available in our copy. (LLM, conf=0.92)
Experimental — accuracy not yet measured
Probably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataIn most included studies (30), one motivational interviewing session was conducted.
“In most studies (30), one motivational interviewing session was conducted.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown dataThe largest included study involved 1726 people and the smallest involved 25 people.
“The largest study involved 1726 people and the smallest involved 25 people.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataMost included studies were conducted in the USA (72).
“The studies were conducted in countries around the world; most were in the USA (72).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataSession durations varied from 10 to 148 minutes per session.
“Session durations varied, from as little as 10 minutes to as long as 148 minutes per session.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataSome included studies conducted up to 9 motivational interviewing sessions.
“There were also studies in which more sessions were conducted, up to 9 sessions.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThis review includes 91 RCTs and two quasi-RCTs.
“This review includes 91 RCTs, and two quasi-RCTs (Bazargan-Hejazi 2005; Freyer-Adam 2008).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataThe sample sizes ranged from 25 to 1726.
“The sample sizes ranged from 25 (Kavanagh 2004) to 1726 (MATCH 1993).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataThree studies focused on cocaine.
“three studies focused on cocaine”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataMotivational interviewing was compared with no intervention in 34 studies.
“Motivational interviewing was compared with: no intervention in 34 studies”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown dataOf the 93 included studies, 72 were published in the USA, five in Australia, four in the United Kingdom, four in the Netherlands, and two in Canada.
“Of the 93 included studies, 72 were published in the USA, five in Australia, four in the United Kingdom, four in the Netherlands and two studies in Canada.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown dataFor the remaining six studies, data were not reported as an effect size and it was not possible to calculate one.
“For the remaining six studies (Field 2010;Parsons 2009;Rohsenow 2004;Stotts 2001;Swogger 2016;Thush 2009), data were not reported in the form of an effect size, and it was not possible to calculate one”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown dataSeventy-three studies were single-site RCTs and 20 were multisite RCTs.
“Seventy-three studies were single-site RCTs and 20 were multisite RCTs.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingnone givenIn 70 studies, the intervention was motivational interviewing.
“In 70 studies, the intervention was motivational interviewing.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataOf the 93 included studies, outcome data were extracted from 87.
“Of the 93 included studies, we were able to extract outcome data from 87.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown dataA total of 168 studies were excluded during full-text review: 85 in the previous version and 83 in the updated version.
“We excluded a total of 168 studies during full-text review: 85 studies in the previous version of the review plus 83 studiesin the updated version.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataTwelve studies examined adolescents.
“12 studies examined adolescents”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataMotivational interviewing was compared with treatment as usual in 23 studies.
“treatment as usual in 23 studies”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataThe duration of the intervention ranged from 10 to 148 minutes per session.
“The duration of the intervention ranged from 10 to 148 minutes per session”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataFive studies included only men.
“Five studies included only men (Gaume 2014; Morgenstern 2009; Murphy 2018; Parsons 2009; Stotts 2006)”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataEleven ongoing studies were identified.
“We identified 11 ongoing studies”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown dataNinety studies reported one comparison and three studies reported two comparisons relevant to the review.
“Ninety studies reported one comparison and three studies reported two comparisons that were relevant to us.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown dataOne study each was published in Germany, Mexico, New Zealand, South Africa, Sweden, and Switzerland.
“One study each was published in Germany, Mexico, New Zealand, South Africa, Sweden, and Switzerland.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataMotivational interviewing was compared with assessment and feedback in nine studies.
“assessment and feedback in nine studies”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataEight studies included both adolescents and young adults.
“eight studies included both adolescents and young adults”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataMotivational interviewing was compared with another active intervention in 30 studies.
“another active intervention in 30 studies”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown dataAlcohol use was addressed in 43 studies, and both alcohol and other drug use in 32 studies.
“Alcohol use was addressed in 43 studies, and both alcohol and other drug use in 32 studies.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataFour studies included only women.
“four included only women (Kelly 2000; Martino 2018; Stein 2010; Winhusen 2008).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe updated review includes 93 studies with 22,776 participants, including 34 new studies published between 2010 and 2022 that examined 9178 participants.
“We included 93 studies with 22,776 participants in this updated review, including 34 new studies published between 2010 and 2022 that examined 9178 participants.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataFifty-four of the studies involved adults.
“Fi yfour of the studies involved adults”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataFive studies included multiple drugs.
“five studies included multiple drugs”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataMost studies included both men and women (84 studies).
“Most studies included both men and women ( 84 studies).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataTen studies focused on the use of cannabis.
“Ten studies focused on the use of cannabis”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataNineteen studies examined only young adults.
“another 19 studies examined only young adults”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataForty-one studies were listed as awaiting classification.
“we listed 41 studies as awaiting classification”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingnone givenThe remaining 23 publications referred to motivational enhancement therapy.
“The remaining 23 publications referred to motivational enhancement therapy.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataFor the other three comparisons, funnel plots appear symmetrical, indicative of no publication bias, although it cannot be ruled out.
“For the other three comparisons (motivational interviewing versus: treatment as usual; assessment and feedback; and other active treatment), the funnel plots appear to be symmetrical, which is indicative of no publication bias, although it cannot be ruled out.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown dataThe number of intervention sessions ranged from one to nine, with one-third of studies (30) involving only one session.
“The number of intervention sessions ranged from one to nine sessions, with one-third of studies (30) involving only one session.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataOur analyses revealed small effect differences for comparisons of motivational interviewing to no intervention and to assessment and feedback.
“Our analyses revealed small effect differences for comparisons of motivational interviewing to no intervention and to assessment and feedback.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataOur analyses showed no differences between motivational interviewing and treatment as usual and another active intervention.
“Our analyses showed no differences between motivational interviewing and treatment as usual and another active intervention.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe evidence was mostly of low or very low certainty; only in three comparisons was the certainty of evidence rated moderate.
“Summary of findings tables 1 to 4 (Summary of findings 1, Summary of findings 2, Summary of findings 3, Summary of findings 4) summarise the results and show that the evidence was mostly of low or very low certainty.Only in three comparisons did we rate the certainty of the evidence as moderate.”
Quote in the paperSubstantial claimMay combine two claims.
Findingnone givenThe studies included in our review come predominantly from high-income countries, with a lack of representation from middle- and low-income countries.
“The studies included in our review come predominantly from high-income countries, with a lack of representation from middle-and low-income countries.”
Quote in the paperSubstantial claimMay combine two claims.
FindingreasoningWe have moderate to no confidence in the evidence, so we need to be cautious about our conclusions.
“We have moderate to no confidence in the evidence, so we need to be cautious about our conclusions.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingnone givenIn the previous version of the review, the effect of motivational interviewing versus no intervention on substance use was moderate.
“while the effect of MI vs. no intervention was moderate in the last version”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataIn the updated review, the effect of motivational interviewing versus no intervention on substance use is small, with low certainty of evidence.
“results in the updated version show a small effect, with low certainty of evidence in both versions.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataThe updated search in November 2022 included 34 new studies in this version of the review.
“We updated the searches in November 2022 and 34 new studies were included in this version.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Findingown dataIncluded studies did not report the secondary outcome of repeat convictions.
“Because studies did not report the secondary outcome of repeat convictions, we did not include this end point in our analyses.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim. May combine two claims.
InterpretationreasoningThe certainty of the research forces the authors to be careful about their conclusions, and new research may change them.
“The certainty of the research forces us to be careful about our conclusions; new research may change them.”
Quote in the paperSubstantial claimMay combine two claims.
Premisenone givenSome of the previous systematic reviews studied the effects of motivational interviewing on groups besides those who use substances, or studied only people who drink alcohol.
“Some of these have studied the effects of motivational interviewing on groups besides those who use substances, or have studied only people who drink alcohol.”
Quote in the paperSubstantial claimMay combine two claims.
Study design and conductown dataThirty studies were judged high risk for incomplete outcome data because losses to follow-up exceeded 20%, reasons were not described, and no intention-to-treat analysis was reported.
“For 30 studies, we judged the risk of bias as high because losses to follow-up were higher than 20%, the reasons for losses were not described, and no intention-to-treat (ITT) analysis was reported.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenReview authors were not blinded to the names of the study authors, institutions, or journal of publication.
“Review authors were not blinded to the names of the study authors, institutions, or journal of publication.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim. May combine two claims.
Study design and conductnone givenThe analyses were based on the intention-to-treat principle; all participants who were randomised were included in the statistical analysis and analysed according to the originally assigned group, regardless of which treatment they received.
“Our analyses were based on the intention-to-treat principle; that is, all participants who were randomised were included in the statistical analysis and analysed according to the originally assigned group, regardless of which treatment (if any) they received.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationMotivational interviewing is regarded as a 'fluid' intervention, which has led to mixed results regarding evidence.
“Thus, it is regarded as a 'fluid' intervention, which has led to mixed results regarding evidence (Björk 2014;Miller 2014).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites Björk 2014
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Miller 2014 source
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductreasoningTwo review authors independently screened titles, abstracts, and full texts, with disagreements resolved through discussion or by a third review author.
“At stage one, working independently, two review authors scanned the titles of each reference.”
- Also stated in: § Selection of studies · plain
“At stage two, working independently, two review authors read the titles and abstracts, and applied the same promotion rules.”
- Also stated in: § Selection of studies · plain
“Working independently, two review authors read the full texts and scored each as 'include' or 'exclude'.”
Quote in the paperNot a substantial claim- Also stated in: § Selection of studies · plain
May combine two claims.
PremisecitationFor substance use, access to and availability of substances, as well as patterns of use, are changing.
“For substance use in particular, access to and availability of substances, as well as patterns of use, are changing (UNODC 2022).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites UNODC 2022
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Classified as probably not a substantial claim. May combine two claims.
Study design and conductnone givenThe main strengths of this review are its exhaustive and systematic search strategy, restriction to randomised controlled trials, assessment of the included studies' risk of bias, and GRADE assessments of evidence for the primary outcomes.
“The main strengths of this review are its exhaustive and systematic search strategy, restriction to randomised controlled trials, assessment of the included studies' risk of bias, and GRADE assessments of evidence for the primary outcomes.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenWhere an adequate number of studies were available (more than 10 studies), the review created funnel plots to assess small-study effects and to explore the possibility of publication bias.
“Where an adequate number of studies were available (more than 10 studies), we created funnel plots to assess small-study effects and to explore the possibility of publication bias.”
Quote in the paperNot a substantial claim- Rests on an assumption: Publication bias poses a significant threat to the validity of any systematic review.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataThirty-four studies were assessed as unclear risk for sequence generation because they did not describe the method.
“We assessed 34 studies as unclear risk as they did not describe the sequence generation method”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductcitationFor the review update, title and abstract screening was independently performed by RS, CD, SU, and SH in two teams of two, using Rayyan.
“For this review update, title and abstract screening was independently performed by RS, CD, SU, and SH (two teams of two), using Rayyan (Ouzzani 2016).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Ouzzani 2016
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataThree studies were assessed as high risk for sequence generation because they did not use adequate methods.
“three studies as high risk because they did not use adequate methods to generate a random allocation.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationIn 2014, Miller and Rollnick described three quality conditions related to intervention content, quality assurance, and intervention fidelity that should be present in a study.
“As a result, in 2014, they described three quality conditions -related to intervention content, quality assurance, and intervention fidelity -that should be present in a study.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Miller 2014 source
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationMiller and Rollnick suggested that therapists should be trained on an appropriate predefined performance criterion prior to treating study participants.
“(2) therapists should be trained on an appropriate predefined performance criterion prior to treating study participants;”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Miller 2014 source
Classified as probably not a substantial claim.
Study design and conductown dataThe review assessed the certainty of the evidence using the GRADE approach for extent of substance use at four follow-up periods, readiness to change, and retention in treatment.
“We assessed the certainty of the evidence using the GRADE approach for the following outcomes: extent of substance use at four follow-up periods (post-intervention, short-, medium-, and long-term follow-up), readiness to change, and retention in treatment.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim.
Study design and conductown dataThe review conducted sensitivity analyses to assess the robustness of the results of the primary outcome by removing studies with a high or unclear risk of bias and including only studies with a low risk of bias.
“We conducted sensitivity analyses to assess the robustness of the results of our primary outcome by removing studies with a high or unclear risk of bias and including only studies with a low risk of bias.”
Quote in the paperSubstantial claimMay combine two claims.
Study design and conductreasoningFor SMDs of 0.5 (medium) and 0.8 (large), the optimal information size is 290 and 116, respectively.
“For SMDs of 0.5 (medium) and 0.8 (large), the OIS is 290 and 116, respectively.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationPatterns of health, disease, and mortality are dynamic and change at both individual and population levels.
“First, patterns of health, disease, and mortality are dynamic and change at both individual and population levels (Cockerham 2021).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Cockerham 2021
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationMiller and Rollnick expressed concerns regarding treatment implementation and fidelity.
“Although Miller and Rollnick embraced this fluidity and indeed encouraged the flexible use of motivational interviewing, they expressed concerns regarding treatment implementation and fidelity.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductcitationAt stage three, full-text review of retrieved articles was independently performed by RS, CD, SU, and SH in two teams of two, using Covidence.
“At stage three, fulltext review of retrieved articles was independently performed by RS, CD, SU, and SH (two teams of two) in Covidence (Covidence 2022).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Covidence 2022
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationMiller and Rollnick suggested that the intervention should include the components that are theoretically and empirically related to its effectiveness.
“Specifically, they suggested that: (1) the intervention should include the components that are theoretically and empirically related to its effectiveness;”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Miller 2014 source
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataSeventeen studies were judged unclear risk for attrition bias because authors stated they used an intention-to-treat analysis but did not report it.
“We judged the risk of attrition bias as unclear for 17 studies because study authors stated they used an ITT analysis but did not report this.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn 41 studies, assessors appeared adequately blinded or results were validated by physiological data, and these were assessed as low risk.
“In a total of 41 studies, the assessors appeared to be adequately blinded or the results were validated by physiological data; we thus assessed these as having a low risk in this domain.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataTwenty-one studies were classified as unclear risk for selective reporting.
“We classified the risk of bias as unclear for 21 studies”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductcitationThe review used the optimal information size to assess whether the sample size was sufficient to derive a statistically significant effect in a meta-analysis.
“We used the optimal information size (OIS) (Pogue 1997) to assess whether the sample size was sufficient to derive a statistically significant effect in a meta-analysis.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Pogue 1997 source
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationMiller and Rollnick suggested that intervention fidelity should be thoroughly documented through reliable coding of therapeutic sessions throughout the study and reported in a manner that allows for direct comparison with competency levels reported in other studies.
“(3) intervention fidelity should be thoroughly documented through reliable coding of therapeutic sessions throughout the study and reported in a manner that allows for direct comparison with competency levels reported in other studies (Miller 2014).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Miller 2014 source
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductcitationTwo review authors independently performed data extraction in Covidence using a data extraction form.
“Working independently, two review authors performed data extraction in Covidence (Covidence 2022), using a data extraction form that contained the following information:”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Covidence 2022
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataTwenty-four studies were classified as low risk for other potential sources of bias.
“We classified 24 studies as low risk of bias”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFifty-four studies were classified as unclear risk for other sources of bias.
“We classified 54 studies as having an unclear risk of other sources of bias”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataTwo authors independently extracted the data for each study, and a third author compared the extraction forms.
“Two authors independently extracted the data for each study; a third author then compared the extraction forms.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataWorking independently in two teams of two, the review authors assessed risk of bias using version one of the Cochrane risk of bias tool.
“Working independently in two teams of two, we assessed risk of bias using version one of the Cochrane risk of bias tool (Higgins 2017).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Higgins 2017
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
Study design and conductnone givenNone of the review authors had a personal, scientific, or financial conflict of interest or expected to profit from the results, thereby reducing the risk of confirmation and significance bias.
“None of the review authors had a personal, scientific, or financial conflict of interest or expected to profit from the results in the form of reviewer decisions or fundraising, thereby reducing the risk of confirmation and significance bias.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
InterpretationreasoningClinical heterogeneity could be due to the populations included, which differed in terms of age, type and severity of substance use, and the substances consumed.
“Clinical heterogeneity could be due to the populations included, which differed in terms of age, type and severity of substance use, and the substances consumed.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningThe certainty for motivational interviewing versus other active intervention was downgraded by one level because randomisation was unclearly reported and there was a high risk of bias in most studies.
“We downgraded by one level because randomisation was unclearly reported and there was a high risk of bias in most studies.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim. May combine two claims.
Study design and conductnone givenTo reduce the risk of bias in the review process, two authors independently screened titles and abstracts, read full texts, extracted data, and assessed risk of bias in the included studies.
“To reduce the risk of bias in the review process, two authors independently screened the titles and abstracts, read the full texts, extracted data, and assessed the risk of bias in the included studies.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationreasoningHeterogeneity might result in inconsistency and imprecision of the treatment effect when the confidence interval includes very different effects and the total number of participants was lower than the optimal information size.
“This might result in inconsistency and imprecision of the treatment effect, when the confidence interval includes very different effects and the total number of participants was lower than the optimal information size.”
Quote in the paperSubstantial claimMay combine two claims.
Study design and conductown dataEvidence was downgraded when the randomisation procedure was not described in detail or when attrition bias was unclear or high, which was the case in many studies.
“We downgraded evidence when the randomisation procedure was not described in detail or when attrition bias was unclear or high, which was the case in many studies.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim.
Study design and conductnone givenThe evidence was downgraded in cases of moderate or substantial unexplained heterogeneity between the treatment effects of different studies.
“We downgraded in cases of moderate or substantial unexplained heterogeneity between the treatment effects of different studies.”
Quote in the paperSubstantial claimMay combine two claims.
Interpretationown dataSubgroup analysis showed that the difference in effect estimates was slightly higher when the substance was alcohol or fewer sessions were conducted, and the effect was smaller when participants used more than one substance.
“Our subgroup analysis showed that the difference in effect estimates was slightly higher when the substance was alcohol or fewer sessions were conducted.Our analysis also showed that the effect was smaller when participants used more than one substance.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Premisenone givenScientific journals impose strict word limits on articles, so important information about the study may not have been reported for that reason.
“Scientific journals impose strict word limits on articles, so important information about the study may not have been reported for that reason.”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationown dataThe substantial heterogeneity in treatment effects when comparing motivational interviewing with no intervention showed a slightly higher benefit for motivational interviewing at post-intervention in studies of alcohol use and a slightly lower benefit in studies with more than one session, but substantial unexplained heterogeneity remained.
“The substantial heterogeneity in treatment effects when comparing motivational interviewing with no intervention showed a slightly higher benefit for motivational interviewing at the post-intervention time point in studies of alcohol use and a slightly lower benefit in studies with more than one motivational interviewing session, but there was still substantial unexplained heterogeneity.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenThe authors contacted authors of published studies and searched ClinicalTrials.gov for unpublished studies to minimise the risk of publication bias.
“Additionally, we contacted authors of published studies and searched on ClinicalTrials.gov to search for unpublished studies to minimise the risk of publication bias.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningIt is not possible to say whether the small differences found in this review were due to an actual lack of efficacy of motivational interviewing or whether motivational interviewing was not implemented as intended.
“Therefore, it is not possible to say whether the small differences found in this review were due to an actual lack of efficacy of motivational interviewing or whether motivational interviewing was not implemented as intended.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationreasoningMost studies were conducted in the USA, which is an important consideration for generalisability, as different social contexts may influence substance-use patterns and the availability and accessibility of an intervention.
“Most studies were conducted in the USA, which is an important consideration in terms of the generalisability of the results, as different social contexts may influence substance-use patterns and the availability and accessibility of an intervention.”
Quote in the paperNot a substantial claim- Rests on an assumption: Different social contexts may influence substance-use patterns and the availability and accessibility of an intervention.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisereasoningThe methodological quality of a study does not necessarily correspond to the quality of reporting of the study.
“The methodological quality of a study does not necessarily correspond to the quality of the reporting of the study.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Alderson 2020, allocation was concealed by central allocation using a secure web-based system, giving low risk of selection bias.
“Central allocation using a secure web-based system.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Bell 2007, blinding of patients and providers was at high risk of performance and detection bias because there was no blinding.
“Blinding (performance bias and detection bias) Patients and providers High risk No blinding of participants and providers.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Aharonovich 2017, assessors were not blinded because drug use was self-assessed in interviews, giving high risk of detection bias.
“Self-assessment of drug use, assessed in interviews.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Alderson 2020, assessors were not blinded because self-reported substance use outcomes were assessed in questionnaires, giving high risk of detection bias.
“Self-reported outcomes on substance use were assessed in questionnaires.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Bell 2007, participants were assigned to condition by a computerized urn randomisation program balancing for age, education, history of head injury with loss of consciousness, gender and enrolment in standard treatments, giving low risk of bias for sequence generation.
“Participants were assigned to condition by a computerized urn randomisation program which balanced for distribution to the groups by the following factors: age, education, presence or absence of history of head injury with loss of consciousness, gender, and enrolment (yes/no) in the six standard treatments...”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationSimilar to our findings, the Foxcro 2016 review reported small differences in favour of motivational interviewing for quantity of alcohol consumed, frequency of alcohol consumption, and alcohol problems at follow-up of less than four months.
“Similar to our findings, the Foxcro 2016 review on motivational interviewing for the prevention of alcohol misuse in young adults reported small differences in favour of motivational interviewing for the quantity of alcohol consumed, the frequency of alcohol consumption, and alcohol problems at follow-up of less than four months.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Foxcro 2016
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductreasoningIn Ball 2007b, the published report included all expected outcomes based on the stated hypotheses, giving low risk of reporting bias.
“The published report included all expected outcomes based on the stated hypotheses.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Bell 2007, 22% were lost to follow-up at 2 months with no intention-to-treat analysis, giving high risk of attrition bias.
“22% were lost to follow-up at 2 months.No ITT analysis.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Ball 2007b, attrition was 32% at 8 weeks and 32% at 16 weeks after treatment, with no significant differences between therapy conditions or condition-by-site interactions in follow-up rates or missing data, giving low risk of attrition bias.
“32% attrition at 8 weeks after treatment.32% attrition at 16 weeks after treatment.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Aharonovich 2017, loss to follow-up was 6.7%, 12.1% and 13.3% at 60 days, 6 months and 12 months respectively, with small differences between conditions, giving low risk of attrition bias.
“6.7%, 12.1%, 13.3% loss to follow-up at 60 days, 6 months, and 12 months, respectively, with small differences between conditions.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Alderson 2020, blinding of participants and providers was not possible, giving high risk of performance/detection bias.
“Blinding not possible for participants or providers;”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductreasoningIn Anton 2005, collateral and biological measurement were used to corroborate self-reports of substance use and there were no differences between groups at baseline, giving low risk of other bias.
“Used collateral and biological measurement to corroborate self-reports of substance use.There were no differences between groups at baseline.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Alderson 2020, all pre-planned outcomes from the protocol were reported, giving low risk of reporting bias.
“All pre-planned outcomes from the protocol were reported in the study.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationFoxcro 2016 found no difference or only a marginal difference for alcohol problems and binge drinking.
“However, no difference or only a marginal difference was found for alcohol problems and bingedrinking.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Foxcro 2016
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
Study design and conductown dataIn Ball 2007b, randomization used a computerized program involving a process of urn allocation, giving low risk of bias for sequence generation.
“The randomisation used a computerized program.(...) This program involved a process of urn allocation.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Bazargan-Hejazi 2005, each of the 3 health promotion advocates performed random allocation for their own enrollees, assigning the first participant by a flip of a coin and alternating thereafter, giving high risk of bias for sequence generation and allocation concealment.
“Each of the 3 health promotion advocates performed random allocation for their own enrollees, assigning the first participant by a flip of a coin, and alternating status thereafter.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductown dataIn Barnett 2007, there was no blinding, giving high risk of performance/detection bias.
“No blinding.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Anton 2005, although there was no blinding, most outcomes were physiological and used to validate self-reports and were not likely to be influenced by lack of blinding, giving low risk of performance/detection bias.
“No blinding, but most outcomes were physiological and also used to validate self-reports, and not likely to be influenced by lack of blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductreasoningIn Barnett 2007, the published report included all expected outcomes based on the stated hypotheses, giving low risk of reporting bias.
“The published report included all expected outcomes based on the stated hypotheses.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationFoxcro 2016 further analyses revealed no clear association between the duration of the motivational interviewing intervention and effect size.
“Further analyses revealed no clear association between the duration of the motivational interviewing intervention and the Cochrane Database of Systematic Reviews effect size.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Foxcro 2016
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Bernstein 2009, selective reporting was at low risk because all expected outcomes were reported.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the stated hypotheses.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Ball 2007b, most outcomes were physiological and used to validate self-reports and were not likely to be influenced by lack of blinding, giving low risk of detection bias.
“Insufficient information to know whether assessors were blinded.But most outcomes were physiological, also used to validate self-reports, and not likely to be influenced by lack of blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Bernstein 2009, random sequence generation was at low risk because randomization was computer-generated in blocks stratified by age.
“Random sequence generation (selection bias) Low risk”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Ball 2007a, although there was no blinding, most outcomes were physiological and used to validate self-reports and were not likely to be influenced by lack of blinding, giving low risk of performance/detection bias.
“No blinding, but most outcomes were physiological, used to validate self-reports, and not likely to be influenced by lack of blinding.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Bernstein 2009, incomplete outcome data was at high risk because 30% were lost at 3 months and 29% at 12 months, not balanced, reasons not stated, and no ITT analysis.
“Incomplete outcome data (attrition bias) All outcomes High risk 30% loss to follow-up at 3 months in the assessed groups, not balanced between groups.29% loss to follow-up at 12 months across all groups, not balanced across groups.Reasons for loss not stated.No ITT analysis, but worstcase scenario analysis.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Alderson 2020, 46.5% of participants were lost at 12 months, balanced across groups, giving high risk of attrition bias.
“46.5% loss at 12 months, balanced across groups.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Aharonovich 2017, participants and providers were not blinded to assignment to MI versus educational control, giving high risk of performance/detection bias.
“No blinding of participants and providers to assignment to MI versus educational control.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Ball 2007b, time spent in training was not balanced across conditions and some contamination of therapy conditions may have occurred, giving high risk of other bias.
“Time spent in training was not balanced across conditions.Some contamination of therapy conditions may have occurred.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Bazargan-Hejazi 2005, enrollees were not followed up by the same health promotion advocate who assessed them initially and patients were told not to reveal their group assignment, giving low risk of detection bias.
“To guard against interviewer bias and to ensure that health promotion advocates were blinded to the patients' randomization allocation for the 3-month follow-up assessments, enrollees were not followed up by the same health promotion advocate who assessed them initially.Patients were notified not to reveal their group assignment to any project staff at any time.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Aharonovich 2017, substance use at 6 and 12 months was reported incompletely, only in figures without standard deviations, giving high risk of reporting bias.
“Substance use at 6 and 12 months was reported incompletely (only in figures, without SD).”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Ball 2007a, alcohol breath testing was used as a check of self-report, giving low risk of other bias.
“Alcohol breath testing used as check of self-report.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Aharonovich 2017, randomization was stratified on drug use severity, depression and unstable housing using urn randomization, giving low risk of bias for sequence generation.
“Randomization was stratified on drug use severity, depression and unstable housing using urn randomization.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Ball 2007a, most outcomes were physiological and used to validate self-reports and were not likely to be influenced by lack of blinding, and the hand-held computer assessment was unlikely to have caused bias, giving low risk of detection bias.
“Insufficient information to know whether assessors were blinded.But most outcomes were physiological, used to validate self-reports, and not likely to be influenced by lack of blinding.The non-blinding may have caused bias regarding the interviews, but the hand-held computer assessment is unlikely to have caused bias.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationFoxcro and colleagues concluded that effect sizes were too small and therefore motivational interviewing has no substantial, meaningful benefit for young adults' alcohol misuse.
“Overall, Foxcro and colleagues concluded that the effect sizes were too small and, therefore, motivational interviewing has no substantial, meaningful benefit for young adults' alcohol misuse.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Foxcro 2016
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductown dataIn Barnett 2007, a research assistant blind to intervention condition conducted the 3- and 12-month follow-up assessments, giving low risk of detection bias.
“A research assistant who was blind to intervention condition conducted the 3-and 12-months follow-up assessments in person, or by phone and mail (...).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Alderson 2020, a computer random generator stratified by placement type, site and age band was used, giving low risk of bias for sequence generation.
“Computer random generator, stratified by placement type (residential / nonresidential), site (local authority) and age band (12 to 14 / over 14).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductreasoningIn Bazargan-Hejazi 2005, the published report included all expected outcomes based on the stated hypotheses, giving low risk of reporting bias.
“The published report included all expected outcomes based on the stated hypotheses.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Bell 2007, blinding of assessors was at high risk because outcomes were self-reported.
“Blinding (performance bias and detection bias) Assessors High risk Self-reported outcomes (alone or with the help of a research assistant).”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Bazargan-Hejazi 2005, only self-reported outcomes were used and the intervention group had a higher rate of drug use and lower mean age at baseline, giving high risk of other bias.
“Only self-reported outcomes.The intervention group had a higher rate of drug use and lower mean age at baseline.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductown dataIn Bazargan-Hejazi 2005, there was no blinding, giving high risk of performance/detection bias.
“No blinding.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Bazargan-Hejazi 2005, attrition was 37% at the 3-month follow-up, balanced between groups, with reasons explained but no intention-to-treat analysis, giving high risk of attrition bias.
“37% attrition at the 3-month follow-up, balanced between groups.Reasons for attrition explained.ITT analysis was not performed.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Anton 2005, most outcomes were physiological and used to validate self-reports and were not likely to be influenced by lack of blinding, giving low risk of detection bias despite uncertainty about assessor blinding.
“Insufficient information to know whether assessors were blinded.But most outcomes were physiological, used to validate self-reports, and not likely to be influenced by lack of blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductreasoningIn Bell 2007, the published report included all expected outcomes based on the stated hypotheses, giving low risk of reporting bias.
“The published report included all expected outcomes based on the stated hypotheses.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Barnett 2007, a random numbers table was used for sequence generation, giving low risk of bias.
“Random numbers table.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductown dataIn Bell 2007, there was no blinding, giving high risk of performance/detection bias.
“No blinding.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Ball 2007b, although there was no blinding, most outcomes were physiological and used to validate self-reports and were not likely to be influenced by lack of blinding, giving low risk of performance/detection bias.
“No blinding, but most outcomes were physiological, also used to validate selfreports, and not likely to be influenced by lack of blinding.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Aharonovich 2017, no sample size calculation was reported, contributing to high risk of other bias.
“no sample size calculation reported”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Anton 2005, attrition was 15% at 12 weeks after treatment, balanced across conditions, with reasons addressed and an intention-to-treat analysis performed, giving low risk of attrition bias.
“15% attrition at 12 weeks after treatment.Balanced across conditions.Reasons addressed.ITT analysis performed.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Aharonovich 2017, there were relevant differences between groups in high-school education (> 10%), contributing to high risk of other bias.
“Relevant differences in high-school education (> 10%)”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationIn contrast to our findings, the Foxcro 2016 analysis revealed a small difference in favour of motivational interviewing for amount of alcohol consumed and frequency of alcohol consumption at follow-up of four months or longer.
“In contrast to our findings, their analysis revealed a small difference in favour of motivational interviewing for the amount of alcohol consumed and the frequency of alcohol consumption at follow-up of four months or longer.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Foxcro 2016
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
Study design and conductown dataIn Bell 2007, other bias was at high risk because only self-reported outcomes were used, there were baseline differences in substance use, and 66% of MI participants did not receive the intervention.
“Other bias High risk Only self-reported outcomes.Baseline differences between intervention groups in substance use.Due to logistical challenges in delivering MI (some MItrained staff were reluctant to take part in the study), 66% of participants randomised to MI did not receive the intervention.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Aharonovich 2017, only self-reported outcomes were used, contributing to high risk of other bias.
“Only self-reported outcomes.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationA subgroup analysis in Foxcro 2016 comparing no intervention with alternative intervention controls at follow-up of less than four months suggests that motivational interviewing may not provide additional benefit compared with other alternative interventions.
“A subgroup analysis comparing no intervention with alternative intervention controls at follow-up of less than four months suggests that motivational interviewing may not provide additional benefit compared with other alternative interventions.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Foxcro 2016
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Bernstein 2009, blinding of patients and providers was at high risk because there was no blinding.
“Blinding (performance bias and detection bias) Patients and providers High risk No blinding.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Bell 2007, incomplete outcome data was at high risk of attrition bias because 59% were lost at 3 months with imbalances, participants who did not receive MI were excluded, and causes were not described.
“Incomplete outcome data (attrition bias) All outcomes High risk Loss to follow-up of a total of 59% of participants at 3 months with imbalances between groups; participants who did not receive MI were excluded (66% of participants who were randomized to MI), causes of loss-to-follow-up were not described.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Ball 2007a, attrition was 7% at 3 weeks after treatment, balanced across conditions, with intention-to-treat analysis used and non-completers accounted for, giving low risk of attrition bias.
“7% attrition at 3 weeks after treatment.Balanced across conditions.Used ITT analysis and the non-completers were all accounted for.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable).
InterpretationreasoningCurrent effect estimates and conclusions may change in light of future trials.
“Current effect estimates and conclusions may change in light of future trials.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Carroll 2006a, blinding of patients and providers was at low risk because although there was no blinding, most outcomes were physiological and used to validate self-reports.
“Blinding (performance bias and detection bias) Patients and providers Low risk No blinding, but most outcomes were physiological, also used to validate selfreports, and not likely to be influenced by lack of blinding.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Carroll 2009, blinding of patients and providers was at low risk because although there was no blinding, most outcomes were physiological and used to validate self-reports.
“Blinding (performance bias and detection bias) Patients and providers Low risk No blinding, but most outcomes were physiological, also used to validate selfreports, and not likely to be influenced by lack of blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn Carey 2006, random sequence generation was at unclear risk because only 'Assigned randomly' was stated.
“Random sequence generation (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn Bien 1993, allocation concealment was at unclear risk because sealed envelopes were used but it is not stated whether they were sequentially numbered or opaque.
“Allocation concealment (selection bias) Unclear risk”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Brown 2015, incomplete outcome data was at high risk because 10%, 15%, 17%, 20%, and 24% were lost at 1, 3, 6, and 9 months with no imbalances, and reasons were not stated.
“Incomplete outcome data (attrition bias) All outcomes High risk 10%, 15%, 17%, 20%, and 24% were lost to follow-up at 1, 3, 6, and 9 months, respectively, with no imbalances between groups; reasons were not stated.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn D'Amico 2018, all planned outcomes were reported, giving low risk of reporting bias.
“Selective reporting (reporting bias) Low risk All planned outcomes were reported (NCT01797835).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Brown 2015, allocation concealment was at low risk because drawing of lots was used.
“Allocation concealment (selection bias) Low risk Drawing of lots (lots for each condition were placed in an envelope and drawn at random by the data analyst to determine the order of cohort group assignment).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Chanut 2007, selective reporting was at low risk because all expected outcomes were reported.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the stated hypotheses.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Carey 2006, blinding of assessors was at high risk because assessors were not blind to condition.
“Blinding (performance bias and detection bias) Assessors High risk Assessors”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Connors 2002, selective reporting was at low risk because all expected outcomes were reported based on the study purposes.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the study purposes.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn De Wildt 2002, although there was no blinding, most outcomes were physiological and used to validate self-reports, giving low risk of performance and detection bias.
“Blinding (performance bias and detection bias) Patients and providers Low risk No blinding, but most outcomes were physiological, also used to validate selfreports, and not likely to be influenced by lack of blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Carey 2011, blinding of patients and providers was at high risk because there was no blinding.
“Blinding (performance bias and detection bias) High risk No blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Bien 1993, incomplete outcome data was at unclear risk because 19% attrition at 6 months was balanced, reasons were explained, but it was unclear whether ITT was performed.
“Incomplete outcome data (attrition bias) All outcomes Unclear risk 19% attrition at 6-month follow-up, balanced between groups.Reasons for attrition explained.Unclear whether ITT was performed.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductreasoningIn Borsari 2005, other bias was at unclear risk because collateral report checked self-report but there were baseline differences in AUDIT, typical BAC, and number of drinks per week.
“Other bias Unclear risk Collateral report as check of self-report.There were baseline differences in AU-DIT, typical BAC, and number of drinks per week.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Chanut 2007, blinding of assessors was at unclear risk because it is not stated whether assessors were blinded.
“Blinding (performance bias and detection bias) Assessors Unclear risk It is not stated whether assessors were blinded.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Carey 2006, selective reporting was at low risk because all expected outcomes were reported.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the stated hypotheses.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Connors 2002, other bias was at low risk because collateral report checked self-report, there were no baseline differences, and no additional sources of bias appeared present.
“Other bias Low risk Collateral report to check on self-report.There were no differences between groups at baseline.No additional sources of bias appear to be present.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Brown 2015, blinding of patients and providers was at high risk because there was no blinding.
“Blinding (performance bias and detection bias) Patients and providers High risk No blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Carroll 2006a, selective reporting was at low risk because all expected outcomes were reported.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the stated hypotheses.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Carroll 2009, blinding of assessors was at low risk because there was insufficient information to know whether assessors were blinded, but most outcomes were physiological and used to validate self-reports.
“Blinding (performance bias and detection bias) Assessors Low risk Insufficient information to know whether assessors were blinded.But most outcomes were physiological, also used to validate self-reports, and not likely to be influenced by lack of blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Carroll 2006a, random sequence generation was at low risk because urn randomisation was used.
“Random sequence generation (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Bien 1993, selective reporting was at low risk because all expected outcomes were reported.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Connors 2002, blinding of patients and providers was at unclear risk because providers could not be blinded but participants could have been.
“Blinding (performance bias and detection bias) Patients and providers Unclear risk Blinding of providers was not possible, but participants could have been blinded.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn De Gee 2014, only self-reported outcomes were available and the sample was small (119 of a planned 140), giving unclear risk of other bias.
“Other bias Unclear risk Only non-physiologically (self-reported) outcomes available; low sample size (out of a planned sample size of 140, 119 participants were recruited).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Brown 2010, selective reporting was at low risk because all expected outcomes were reported.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the stated hypotheses.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Colby 2018, incomplete outcome data was at low risk because follow-up was 97% and 96% at 6 weeks and 3 months, respectively, with no differences between groups.
“Incomplete outcome data (attrition bias) All outcomes Low risk Follow-up of 97% and 96% at 6 weeks and 3 months, respectively, with no differences between groups.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing).
Study design and conductreasoningIn Connors 2002, random sequence generation was at unclear risk because only 'randomly assigned' was stated.
“Random sequence generation (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Carroll 2009, other bias was at unclear risk because only self-reported outcomes were used and differences at baseline were not reported.
“Other bias Unclear risk Only self-reported outcomes.Differences at baseline were not reported.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Carroll 2006b, blinding of assessors was at low risk because there was insufficient information to know whether assessors were blinded, but most outcomes were physiological and used to validate self-reports.
“Blinding (performance bias and detection bias) Assessors Low risk Insufficient information to know whether assessors were blinded.But most outcomes were physiological, also used to validate self-reports, and not likely to be influenced by lack of blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Colby 2018, other bias was at unclear risk because no physiological outcomes were reported, there were no baseline differences, and no additional sources of bias appeared present.
“Other bias Unclear risk No physiological outcomes reported.No differences between groups at baseline.No additional sources of bias appear to be present.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Brown 2015, random sequence generation was at low risk because a computer random number generator was used.
“Random sequence generation (selection bias) Low risk Computer random number generator”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductcitationIn Brown 2010, blinding of patients and providers was at low risk because participants, interviewers, statistician, and investigators were blind to assignment.
“Blinding (performance bias and detection bias) Patients and providers Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductreasoningIn Carroll 2006a, blinding of assessors was at unclear risk because there was insufficient information to know whether assessors were blinded, but most outcomes were physiological and used to validate self-reports.
“Blinding (performance bias and detection bias) Assessors Unclear risk Insufficient information to know whether assessors were blinded.But most outcomes were physiological, also used to validate self-reports, and not likely to be influenced by lack of blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Carey 2006, incomplete outcome data was at unclear risk because 3% were lost at 1 month, 23% at 6 months, and 22% at 12 months, balanced across conditions, reasons were addressed but not detailed, and it was unclear whether ITT was used.
“Incomplete outcome data (attrition bias) All outcomes Unclear risk 3% loss to follow-up at one month, 23% at 6 months, and 22% at 12 months.Balanced across conditions.Reasons for missing data addressed but not detailed.Unclear whether ITT analysis was used.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Borsari 2005, selective reporting was at low risk because all expected outcomes were reported.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the stated hypotheses.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Colby 2018, blinding of assessors was at high risk because alcohol consumption was self-reported via self-administered interactive computer programs.
“Blinding (performance bias and detection bias) Assessors High risk Self-reported alcohol consumption via self-administered interactive computer programs.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Borsari 2012, incomplete outcome data was at low risk because 6% were lost at 3 and 9 months and 9% at 6 months with no imbalances.
“Incomplete outcome data (attrition bias) All outcomes Low risk 6% loss to follow-up at 3 and 9 months, 9% at 6 months with no imbalances between groups.Reasons for loss not stated.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn D'Amico 2018, allocation was adjusted using a random number generator, giving low risk of selection bias from sequence generation.
“Random sequence generation (selection bias) Low risk”
- Also stated in: § Carroll 2006b · plain
“Allocation was adjusted using a random number generator.”
Quote in the paperNot a substantial claim- Also stated in: § Carroll 2006b · plain
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Colby 2018, random sequence generation was at low risk because urn randomisation was stratified by age, gender, education status, and past-month heavy drinking frequency.
“Random sequence generation (selection bias) Low risk Urn randomisation, stratified by age, gender, education status, and pastmonth heavy drinking frequency.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductreasoningIn Copeland 2001, the published report included all expected outcomes based on the stated hypotheses, giving low risk of reporting bias.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the stated hypotheses.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Bernstein 2009, other bias was at high risk because only self-reported outcomes were used and the intervention group used marijuana on more days per month at baseline.
“Other bias High risk Only self-reported outcomes.The intervention group used marijuana on more days per month than the assessed control (AC) group at baseline.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Borsari 2005, blinding of patients and providers was at high risk because there was no blinding.
“Blinding (performance bias and detection bias) Patients and providers High risk No blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Colby 2018, blinding of patients and providers was at high risk because there was no blinding of participants and providers.
“Blinding (performance bias and detection bias) Patients and providers High risk No blinding of participants and providers.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Brown 2010, incomplete outcome data was at low risk because 7% were lost after randomisation and intervention, excluded from further analyses without ITT, no reasons were given, and a further 6% were lost with data estimated.
“Incomplete outcome data (attrition bias) All outcomes Low risk 7% were lost after randomisation and intervention.They were excluded from further analyses (no ITT analysis).No reasons for attrition.A further 6% was lost and data were estimated.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Carey 2011, incomplete outcome data was at high risk because 5%, 61%, and 31% were lost at 1, 6, and 12 months with imbalances, and the delayed control group had only 1-month follow-up data.
“Incomplete outcome data (attrition bias) All outcomes High risk 5%, 61%, and 31% loss to follow-up at 1, 6, and 12 months with imbalances between three groups with follow-up over 12 months.For the delayed control group, only the 1-month follow-up data were available (2% loss to follow-up).”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Carroll 2009, incomplete outcome data was at high risk because 28% were lost to follow-up, reasons were not described but similar between groups, and no ITT analysis was done even though an intention-to-treat sample was reported.
“Incomplete outcome data (attrition bias) All outcomes High risk 28% loss to follow-up.Reasons for attrition not described but similar between groups.No ITT analysis even though they reported an intention-to-treat sample.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Borsari 2005, blinding of assessors was at unclear risk because it is not stated whether assessors were blinded.
“Blinding (performance bias and detection bias) Assessors Unclear risk It is not stated whether the assessors were blinded.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Bien 1993, blinding of assessors was at low risk because assessors were kept blind to group assignment.
“Blinding (performance bias and detection bias) Assessors Low risk Assessors”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Copeland 2001, blinding of patients and providers was not performed, giving high risk of performance and detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk No blinding.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Carroll 2006b, other bias was at low risk because urine toxicology screens and breath samples checked self-report, there were no baseline differences, and no additional sources of bias appeared present.
“Other bias Low risk Urine toxicology screens and breath samples to check on self-report.There were no differences between groups at baseline.No additional sources of bias appear to be present.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn De Gee 2014, stratified (by region) block randomisation was used, giving low risk of selection bias from sequence generation.
“Random sequence generation (selection bias) Low risk Stratified (by region) block randomisation (lists generated in Excel 2007, applied through a Microsoft Access database).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn Bien 1993, random sequence generation was at unclear risk because assignment was random but the method was not described.
“Random sequence generation (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductreasoningIn Borsari 2005, random sequence generation was at unclear risk because only 'Randomly assigned' was stated.
“Random sequence generation (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Carroll 2009, random sequence generation was at low risk because urn allocation was used.
“Random sequence generation (selection bias) Low risk Urn allocation.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Borsari 2012, random sequence generation was at low risk because urn randomisation was used.
“Random sequence generation (selection bias) Low risk Urn randomisation”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Bien 1993, blinding of patients and providers was at unclear risk because providers could not be blinded but participants could have been.
“Blinding (performance bias and detection bias) Patients and providers Unclear risk Blinding of providers was not possible, but participants could have been blinded.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Borsari 2012, allocation concealment was at low risk because an on-site computer with a locked file was used.
“Allocation concealment (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Carroll 2006b, selective reporting was at low risk because all expected outcomes were reported.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the stated hypotheses.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Colby 2018, selective reporting was at high risk because results on all pre-planned primary outcomes were reported but not for secondary outcomes.
“Selective reporting (reporting bias) High risk Results on all pre-planned primary outcomes (NCT0154602) were reported, but not for the secondary outcomes.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Chanut 2007, random sequence generation was at low risk because urn randomisation was used.
“Random sequence generation (selection bias) Low risk Urn randomisation:”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Carroll 2006a, other bias was at unclear risk because urine and breath samples checked self-report, but time spent in training was not balanced across conditions and clinicians assigned to MI received more training and supervision.
“Other bias Unclear risk Urine and breath samples to check on self-report.Time spent in training was not balanced across conditions, and clinicians assigned to MI received more training and supervision.There were no differences between groups at baseline.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Carey 2011, other bias was at unclear risk because only self-reported outcomes were used, no sample size analysis or baseline data per group were reported, and the delayed-intervention control condition provided only 1-month follow-up data.
“Other bias Unclear risk Only self-reported outcomes; no sample size analysis or baseline data per group reported; delayed-intervention control condition provided only 1month follow-up data.No additional sources of bias appear to be present.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn De Wildt 2002, attrition was 30% at 6-month follow-up, balanced, with reasons stated and intention-to-treat analysis, giving low risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk 30% attrition at 6-month follow-up.Balanced dropout and reasons for dropout stated.ITT analysis completed.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn D'Amico 2018, loss to follow-up was 26%, 16% and 20% in the intervention group and 39%, 21% and 19% in the control group at 3, 6 and 12 months, with intention-to-treat analysis and multiple imputation, giving low risk of attrition bias.
“Loss to follow-up in the intervention group was 26% at 3 months, 16% at 6 months, and 20% at 12 months.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductown dataIn De Gee 2014, outcomes were only self-reported via questionnaires, giving high risk of detection bias.
“Blinding (performance bias and detection bias) Assessors High risk Only self-reported outcomes via questionnaires.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductnone givenIn Brown 2010, blinding of assessors was at low risk because participants, interviewers, statistician, and investigators were blind to assignment.
“Blinding (performance bias and detection bias) Assessors Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn De Wildt 2002, the published report included all expected outcomes based on the study hypotheses, giving low risk of reporting bias.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the study hypotheses.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Chanut 2007, incomplete outcome data was at unclear risk because attrition was 22% at 3 months and 29% at 6 months, balanced across groups, reasons were not reported, and use of ITT was reported but it was unclear whether all analyses used ITT.
“Incomplete outcome data (attrition bias) All outcomes Unclear risk Attrition was 22% at 3 months and 29% at 6 months.Balanced across groups.Reasons for loss to follow-up not reported.Use of ITT analysis was reported, but it is unclear whether all reported analyses used ITT.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Copeland 2001, 34% of randomised participants did not complete the final survey (unequal numbers) and no intention-to-treat analysis was done, giving high risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes High risk 34% of those randomised did not complete the final survey (unequal numbers).”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn De Gee 2014, loss to follow-up differed between groups (22.4% in the MI intervention group versus 13.1% in the control condition), giving high risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes High risk Differences in loss-to follow-up between groups (22.4% loss to follow-up in the intervention group with MI versus 13.1% in the control condition).”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Carey 2006, other bias was at low risk because collateral report checked self-report, there were no baseline differences, and no additional sources of bias appeared present.
“Other bias Low risk Collateral report as check of self-report.There were no differences between groups at baseline.No additional sources of bias appear to be present.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Borsari 2012, other bias was at unclear risk because only self-reported outcomes were used, 9% of randomised participants did not receive the intervention, and baseline differences and sample-size calculation were not reported.
“Other bias Unclear risk Only self-reported outcomes.9% of randomised participants did not receive the intervention.Differences between groups at baseline and sample-size calculation were not reported.No additional sources of bias appear to be present.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Carroll 2009, selective reporting was at low risk because all expected outcomes were reported.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the stated hypotheses.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn D'Amico 2018, outcomes were self-reported, giving high risk of detection bias from lack of assessor blinding.
“Blinding (performance bias and detection bias) Assessors High risk Self-reported outcomes”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Copeland 2001, only self-reported outcomes were available and differences between groups at baseline were not reported, giving unclear risk of other bias.
“Other bias Unclear risk Only self-reported outcomes.Differences between groups at baseline were not reported.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn D'Amico 2018, blinding of providers was not possible, giving high risk of performance and detection bias.
“Blinding of providers was not possible.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Chanut 2007, blinding of patients and providers was at unclear risk because providers could not be blinded but participants could have been.
“Blinding (performance bias and detection bias) Patients and providers Unclear risk Blinding of providers was not possible, but participants could have been blinded.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Brown 2015, blinding of assessors was at low risk because self-reported daily alcohol and drug use was highly related to urine THC results.
“Blinding (performance bias and detection bias) Assessors Low risk Self-report of daily alcohol and drug use via interview.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Brown 2010, random sequence generation was at low risk because computerised urn randomisation was used.
“Random sequence generation (selection bias) Low risk Computerised urn randomisation”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn De Gee 2014, participants were blind to their allocated condition, giving low risk of performance and detection bias.
“Blinding (performance bias and detection bias) Patients and providers Low risk”
- Also stated in: § Carroll 2006b · plain
“Participants were blind to the condition to which they had been allocated, only after the baseline assessment had been completed were the results of the randomization communicated to prevention workers”
Quote in the paperNot a substantial claim- Also stated in: § Carroll 2006b · plain
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Carroll 2006b, incomplete outcome data was at unclear risk because 38% attrition at 3 months and 21% at 6 months showed imbalance, reasons were not stated, but ITT analysis was performed.
“Incomplete outcome data (attrition bias) All outcomes Unclear risk 38% attrition at 3 months and 21% attrition at 6 months.Imbalance between groups.Reasons for missing data not stated.ITT analysis was performed.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Bien 1993, other bias was at low risk because collateral report checked self-report, there were no baseline differences, and no additional sources of bias appeared present.
“Other bias Low risk Collateral report as check of self-report.There were no differences between groups at baseline.No additional sources of bias appear to be present.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductreasoningIn Brown 2010, other bias was at low risk because threat of invalidity in self-report was addressed by corroboration from biomarkers and measurement of social desirability, and there were no baseline differences.
“Other bias Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Borsari 2012, selective reporting was at high risk because heavy drinking days were only reported in figures without numbers and exact values.
“Selective reporting (reporting bias) High risk Heavy drinking days were only reported in figures without numbers and exact values.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Chanut 2007, other bias was at unclear risk because collaterals were used to verify self-report but there were baseline differences in days of hazardous drinking and the Drug Abuse Screening Test.
“Other bias Unclear risk Used collaterals to verify self-report.There were baseline differences in days of hazardous drinking and the Drug Abuse Screening Test.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Borsari 2005, incomplete outcome data was at high risk because 11% were lost at 3 months and 25% at 6 months, balance was not stated, reasons were not stated, and ITT was not performed.
“Incomplete outcome data (attrition bias) All outcomes High risk 11% loss to follow-up after 3 months and 25% lost to follow-up after 6 months.Balance in numbers not stated.Reasons for missing data not stated.ITT analysis not performed.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Brown 2015, other bias was at unclear risk because no sample size calculation was reported, very few baseline criteria were reported, and valid urine toxicology results were obtained for only about half the sample.
“Other bias Unclear risk No sample size calculation reported; very few baseline criteria reported; valid urine toxicology results were obtained for 52.3%, 46.4%, and 50.3% of the sample at 1, 6, and 12-month follow-ups.No additional sources of bias appear to be present.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Connors 2002, blinding of assessors was at unclear risk because it is not stated whether assessors were blinded.
“Blinding (performance bias and detection bias) Assessors Unclear risk It is not stated whether the assessors were blinded.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Borsari 2012, blinding of patients and providers was at high risk because there was no blinding of participants and providers.
“Blinding (performance bias and detection bias) Patients and providers High risk No blinding of participants and providers.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Carey 2011, selective reporting was at unclear risk because no published protocol was available.
“Selective reporting (reporting bias) Unclear risk No published protocol available.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Carey 2006, blinding of patients and providers was at high risk because there was no blinding.
“Blinding (performance bias and detection bias) Patients and providers High risk No blinding.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Feldstein 2007, loss to follow-up was 7% at 2 months, balanced across groups with reasons stated, giving low risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk 7% loss to follow-up at 2 months, balanced across groups.Reasons stated.No ITT analysis.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Feldstein 2007, undergraduate assistants blind to randomisation collected participant data at follow-up, giving low risk of detection bias.
“Blinding (performance bias and detection bias) Assessors Low risk”
- Also stated in: § Study characteristics · plain
“Undergraduate assistants blind to the randomization collected participant data at the follow-up.”
Quote in the paperNot a substantial claim- Also stated in: § Study characteristics · plain
May combine two claims.
Study design and conductown dataIn Kahler 2004, attrition was 4%, 4%, 6%, 6%, 12% and 12% at 1, 2, 3, 4, 5 and 6 months' follow-up, giving low risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk 48 were randomised.Attrition was 4%, 4%, 6%, 6%, 12%, and 12% at 1, 2, 3, 4, 5, and 6 months' follow-up, respectively.No reasons for insufficient data reported.No ITT analysis performed.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Dieperink 2014, stratified block randomisation using random allocation software by the study statistician was used, giving low risk of selection bias from allocation concealment.
“Allocation concealment (selection bias) Low risk Stratified block randomisation using random allocation software by the study statistician.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Emmen 2005, the published report included all expected outcomes based on the study hypotheses, giving low risk of reporting bias.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the study hypotheses.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Marijuana Treatment Project 2004, allocation concealment was at unclear risk of bias.
“Allocation concealment (selection bias) Unclear risk Insufficient information to permit judgment.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Emmen 2005, loss to follow-up was 9% at 6 months, balanced, with reasons stated and intention-to-treat analysis, giving low risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk 9% loss to follow-up at 6 months.Balanced dropout.Reasons stated.ITT analysis performed.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Kadden 2007, 17% were lost to follow-up with reasons stated, attrition differed across groups and no intention-to-treat analysis was done, giving unclear risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Unclear risk 17% lost to follow-up with reasons stated.Different attrition across groups.No ITT.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Feldstein 2007, a random number list was used for sequence generation, giving low risk of selection bias.
“Random sequence generation (selection bias) Low risk Used a random number list.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Maisto 2001, random sequence generation was at low risk of bias.
“Random sequence generation (selection bias) Low risk Random numbers table.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Kavanagh 2004, attrition was 4% at 6 months and 32% at 12 months, balanced, with intention-to-treat analysis, giving unclear risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Unclear risk Attrition was 4% at 6 months and 32% at 12 months.Balanced.We do not know the attrition at 6 weeks and 3 months.Reasons for loss were not reported.ITT analysis was performed.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Kay-Lambkin 2009, other bias was at low risk of bias.
“Other bias Low risk Collateral report to check on self-report.There were no differences between groups at baseline.No additional sources of bias appear to be present.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Emmen 2005, balanced block randomisation with sealed envelopes was used to generate the allocation sequence, giving low risk of selection bias.
“Random sequence generation (selection bias) Low risk”
- Also stated in: § Study characteristics · plain
“(...) balanced block randomisation.The main researcher (M.J.E) used sealed envelopes to generate the allocation sequence.”
Quote in the paperNot a substantial claim- Also stated in: § Study characteristics · plain
May combine two claims.
Study design and conductown dataIn Feldstein Ewing 2021, changes were reported at 6-month follow-up but not at 3 and 12 months as planned in the protocol, giving high risk of reporting bias.
“Selective reporting (reporting bias) High risk Changes were reported at 6-month follow-up, but not at 3 and 12 months as planned in the protocol.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Dieperink 2014, loss to follow-up was 16% at 6 months with no differences between groups and causes described, giving low risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk Loss to follow-up of 16% of participants at 6 months with no differences between groups; causes were described.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Kelly 2000, other bias was at unclear risk of bias.
“Other bias Unclear risk No baseline values reported for all participants or participants with pre-treatment scans; no sample size calculation.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Dermen 2011, there was no blinding of participants and providers, giving high risk of performance and detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk No blinding of participants and providers.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Maisto 2001, incomplete outcome data was at unclear risk of bias.
“Incomplete outcome data (attrition bias) All outcomes Unclear risk Attrition was 5%, 8%, 14%, 15%, and 17% at 1 month, 3 months, 6 months, 9 months, and 12 months, respectively.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataFor Marsden 2006, allocation concealment was at unclear risk of bias.
“Allocation concealment (selection bias) Unclear risk Insufficient information to permit judgement.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Kay-Lambkin 2009, random sequence generation was at unclear risk of bias.
“Random sequence generation (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Kadden 2007, computerised urn randomisation was used, giving low risk of selection bias from sequence generation.
“Random sequence generation (selection bias) Low risk Computerised urn randomisation.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductreasoningIn Gaume 2014, allocation concealment was achieved by a priori generated random orders of badge numbers, giving low risk of selection bias.
“Allocation concealment (selection bias) Low risk”
- Also stated in: § Freyer-Adam 2008 · plain
“Study inclusion happened during the conscription process for the Swiss military.During this process, conscripts were grouped by 50 and wore a badge numbered from 1 to 50.”
Quote in the paperNot a substantial claim- Also stated in: § Freyer-Adam 2008 · plain
May combine two claims.
Study design and conductown dataIn Kahler 2004, research assistants were blind to treatment assignment of individuals and cohorts, giving low risk of detection bias.
“Blinding (performance bias and detection bias) Assessors Low risk”
- Also stated in: § Freyer-Adam 2008 · plain
“RAs (research assistants) were blind to treatment assignment of individuals and cohorts.”
Quote in the paperNot a substantial claim- Also stated in: § Freyer-Adam 2008 · plain
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningFor Marijuana Treatment Project 2004, other bias was at unclear risk of bias.
“Other bias Unclear risk Collateral interviews and urine specimens to check on self-report.Numbers of sessions were confounded with differential content and process.Different expectancies of success were created by the differences in treatment length.There were no differences between groups at baseline.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Gaume 2014, a computer random number generator was used, giving low risk of selection bias from sequence generation.
“Random sequence generation (selection bias) Low risk Computer random number generator.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataFor Marijuana Treatment Project 2004, blinding of assessors was at unclear risk of bias.
“Blinding (performance bias and detection bias) Assessors Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductown dataIn Feldstein 2007, there was no blinding, giving high risk of performance and detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk No blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductown dataIn Kahler 2004, there was no blinding, giving high risk of performance and detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk No blinding.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Emmen 2005, serum carbohydrate-deficient transferrin was measured as biological data and there were no differences between groups at baseline, giving low risk of other bias.
“Other bias Low risk Serum carbohydrate-deficient transferrin (CDT) was measured (biological data).There were no differences between groups at baseline.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Field 2010, blinding was not possible, giving high risk of performance and detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk Blinding not possible.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Marijuana Treatment Project 2004, random sequence generation was at low risk of bias.
“Random sequence generation (selection bias) Low risk Urn randomisation.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningFor Maisto 2001, other bias was at low risk of bias.
“Other bias Low risk Collateral reports were used to check self-report.There were no differences between groups at baseline.No additional sources of bias appear to be present.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductreasoningIn Kavanagh 2004, participants were allocated randomly using a separate table of random permutations for each site, giving low risk of selection bias from sequence generation.
“Random sequence generation (selection bias) Low risk”
- Also stated in: § Freyer-Adam 2008 · plain
“(...) participants were allocated randomly to conditions using a separate table of random permutations for each site.”
Quote in the paperNot a substantial claim- Also stated in: § Freyer-Adam 2008 · plain
May combine two claims.
Study design and conductown dataIn Dermen 2011, follow-up completion rates at 3, 6, 9, 12 and 15 months were 95%, 94%, 92%, 91% and 91% and did not differ significantly by condition, giving low risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk Follow-up completion rates for the 3, 6, 9, 12, and 15-month follow-ups were 95%, 94%, 92%, 91%, and 91%, respectively, and did not differ significantly by condition.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Kelly 2000, selective reporting was at unclear risk of bias.
“Selective reporting (reporting bias) Unclear risk No protocol available.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductown dataIn Kadden 2007, the published report included all expected outcomes based on the study purposes, giving low risk of reporting bias.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the study purposes.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Kadden 2007, urine samples were collected to check self-report and there were no differences between groups at baseline, giving low risk of other bias.
“Other bias Low risk Urine samples were collected to check on self-report.There were no differences between groups at baseline.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenFor Kelly 2000, blinding of patients and providers was at high risk of bias.
“Blinding (performance bias and detection bias) Patients and providers High risk Insufficient information to permit judgement.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenFor Maisto 2001, selective reporting was at low risk of bias.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the study hypotheses.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Kavanagh 2004, the final assessment was undertaken by research staff blind to treatment conditions, giving low risk of detection bias.
“Blinding (performance bias and detection bias) Assessors Low risk”
- Also stated in: § Freyer-Adam 2008 · plain
“The final assessment was undertaken by research staff who were blind to treatment conditions.”
Quote in the paperNot a substantial claim- Also stated in: § Freyer-Adam 2008 · plain
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Dieperink 2014, Pocock & Simon's minimisation method was used for sequence generation, giving low risk of selection bias.
“Random sequence generation (selection bias) Low risk Pocock & Simon's minimisation method.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Kay-Lambkin 2009, a permuted block randomisation approach was used, giving low risk of selection bias from sequence generation.
“Random sequence generation (selection bias) Low risk”
- Also stated in: § Freyer-Adam 2008 · plain
“A permuted block randomisation approach was used so that the distribution of participants across treatment conditions could be maintained regardless of the final sample”
Quote in the paperNot a substantial claim- Also stated in: § Freyer-Adam 2008 · plain
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningFor Logan 2015, blinding of assessors was at high risk of bias.
“Blinding (performance bias and detection bias) Assessors High risk Physiological measurement of blood alcohol content and urine samples provided immediate screen to ensure that participants were not intoxicated at the time of MRI data collection, but did not serve as a control for self-reported substance use.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Dieperink 2014, there was no blinding of participants and providers, giving high risk of performance and detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk No blinding of participants and providers.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Marijuana Treatment Project 2004, selective reporting was at low risk of bias.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the study hypotheses.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Dieperink 2014, all measures were administered by a research assistant blinded to the randomised condition, giving low risk of detection bias.
“Blinding (performance bias and detection bias) Assessors Low risk”
- Also stated in: § Study characteristics · plain
“All measures were administered by a research assistant who was blinded to the randomized condition, measurement of physiological data.”
Quote in the paperNot a substantial claim- Also stated in: § Study characteristics · plain
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Kelly 2000, allocation concealment was at unclear risk of bias.
“Allocation concealment (selection bias) Unclear risk Not reported.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Kavanagh 2004, only self-reported outcomes were available and groups were significantly different at baseline, giving high risk of other bias.
“Other bias High risk Only self-reported outcomes.Groups were significantly different at baseline.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenFor Kay-Lambkin 2009, selective reporting was at low risk of bias.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the study hypotheses.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Kay-Lambkin 2009, allocation concealment was at unclear risk of bias.
“Allocation concealment (selection bias) Unclear risk Insufficient information to permit judgement.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Freyer-Adam 2008, the staff was not blind to the study group to which participants had been assigned, giving high risk of detection bias.
“Blinding (performance bias and detection bias) Assessors High risk”
- Also stated in: § Study characteristics · plain
“(...) the staff was not blind to the study group to which the participants had been assigned.”
Quote in the paperNot a substantial claim- Also stated in: § Study characteristics · plain
May combine two claims.
Study design and conductown dataIn Freyer-Adam 2008, loss to follow-up was 29% at 12 months, not balanced, with reasons provided and no intention-to-treat analysis, giving high risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes High risk 29% loss to follow-up at 12 months, not balanced, reasons provided.No ITT analysis.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductreasoningIn Freyer-Adam 2008, the published report included all expected outcomes based on the stated hypotheses, giving low risk of reporting bias.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the stated hypotheses.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Logan 2015, allocation concealment was at unclear risk of bias.
“Allocation concealment (selection bias) Unclear risk Not reported.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenFor Maisto 2001, allocation concealment was at low risk of bias.
“Allocation concealment (selection bias) Low risk”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Emmen 2005, although there was no blinding, most outcomes were physiological and used to validate self-reports, giving low risk of performance and detection bias.
“Blinding (performance bias and detection bias) Patients and providers Low risk No blinding, but most outcomes were physiological, also used to validate selfreports, and not likely to be influenced by lack of blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductown dataIn Freyer-Adam 2008, there was no blinding, giving high risk of performance and detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk No blinding.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Freyer-Adam 2008, only self-reported outcomes were available and there were differences between groups at baseline on satisfaction with health, age and having an intimate partner, giving high risk of other bias.
“Other bias High risk Only self-reported outcomes.Because staff became more experienced over time, they might have recruited different patients in the first period -when they recruited the controls -than in the later period -when they recruited to the intervention groups.There were differences between groups at baseline on satisfaction with health, age, and having an intimate partner.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Gaume 2014, follow-up was 82% at 3 months with no difference between groups, giving low risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk 82% follow-up at 3 months with no difference between groups.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductreasoningIn Feldstein 2007, the published report included all expected outcomes based on the stated hypotheses, giving low risk of reporting bias.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the stated hypotheses.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataFor Maisto 2001, blinding of patients and providers was at high risk of bias.
“Blinding (performance bias and detection bias) Patients and providers High risk No blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataFor Maisto 2001, blinding of assessors was at unclear risk of bias.
“Blinding (performance bias and detection bias) Assessors Unclear risk It is not stated whether the assessors were blinded.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenFor Logan 2015, blinding of patients and providers was at high risk of bias.
“Blinding (performance bias and detection bias) Patients and providers High risk Insufficient information to permit judgement.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductown dataIn Gaume 2014, outcomes were self-reported via questionnaires, giving high risk of detection bias.
“Blinding (performance bias and detection bias) Assessors High risk Self-reported outcomes via questionnaires.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductown dataIn Kavanagh 2004, there was no blinding, giving high risk of performance and detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk No blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenFor Marsden 2006, random sequence generation was at unclear risk of bias.
“Random sequence generation (selection bias) Unclear risk”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Dermen 2011, follow-up assessments were conducted by same-gender interviewers blind to experimental condition and reports were compared with collateral reports, giving low risk of detection bias.
“Blinding (performance bias and detection bias) Assessors Low risk Self-reported outcomes; follow-up assessments were conducted by same-gender interviewers blind to experimental condition; reports were compared to collateral reports with no relevant differences.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningFor Marsden 2006, blinding of patients and providers was at unclear risk of bias.
“Blinding (performance bias and detection bias) Patients and providers Unclear risk No blinding but the outcome measurements were not likely to be influenced by lack of blinding due to validation with physiological measurement.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductreasoningIn Kahler 2004, the published report included all expected outcomes based on the stated hypotheses, giving low risk of reporting bias.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the stated hypotheses.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn De Wildt 2002, 23% of participants consulted another professional for alcohol-related problems during treatment, giving high risk of other bias.
“Other bias High risk 23% of participants consulted some other professional for alcohol-related problems during the treatment.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Field 2010, sequentially numbered opaque envelopes opened after completion of the baseline assessment were used, giving low risk of selection bias from allocation concealment.
“Allocation concealment (selection bias) Low risk Sequentially numbered opaque envelopes, opened after completion of baseline assessment.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Field 2010, follow-up was 94%, 91% and 88% of participants over 3, 6 and 12 months with no differences between groups in numbers and causes for loss, giving low risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk Follow-up of 94%, 91%, and 88% of participants over 3, 6, and 12 months, respectively, with no differences between groups in numbers and causes for loss to follow-up.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Feldstein Ewing 2021, outcomes were self-reported on a laptop via audio computer-assisted self-interview, giving high risk of detection bias.
“Blinding (performance bias and detection bias) Assessors High risk Self-reported outcomes”
- Also stated in: § Study characteristics · plain
“on a laptop via audio computer-assisted self-interview.”
Quote in the paperNot a substantial claim- Also stated in: § Study characteristics · plain
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Kay-Lambkin 2009, blinding of assessors was at unclear risk of bias.
“Blinding (performance bias and detection bias) Assessors Unclear risk It is not stated whether the assessors were blinded.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Feldstein Ewing 2021, a gender-stratified random number generator was used, giving low risk of selection bias from sequence generation.
“Random sequence generation (selection bias) Low risk Gender-stratified random number generator.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenFor Marsden 2006, blinding of assessors was at low risk of bias.
“Blinding (performance bias and detection bias) Assessors Low risk”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Feldstein Ewing 2021, follow-up was 87% at 6 months, giving low risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk 87% follow-up at 6 months.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Study design and conductown dataIn Gaume 2014, blinding of participants was not possible, giving high risk of performance and detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk Blinding of participants not possible.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningIn Freyer-Adam 2008, randomisation was conducted by time-frame based on the date of admission, giving high risk of selection bias from sequence generation.
“Random sequence generation (selection bias) High risk”
- Also stated in: § Study characteristics · plain
“(...) randomisation was conducted by time-frame, based on the date of admission.”
Quote in the paperNot a substantial claim- Also stated in: § Study characteristics · plain
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Dermen 2011, the allocation sequence was prepared in advance by the project director using a random number table, giving low risk of selection bias from sequence generation.
“Random sequence generation (selection bias) Low risk”
- Also stated in: § Study characteristics · plain
“Prepared in advance by the project director using a random number table.”
Quote in the paperNot a substantial claim- Also stated in: § Study characteristics · plain
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Logan 2015, other bias was at unclear risk of bias.
“Other bias Unclear risk No baseline values reported for all participants or participants with pre-treatment scans; no sample size calculation.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Field 2010, a random number generator was used, giving low risk of selection bias from sequence generation.
“Random sequence generation (selection bias) Low risk Random number generator.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Dermen 2011, allocation concealment used envelopes prepared in advance by the project director, giving low risk of selection bias.
“Allocation concealment (selection bias) Low risk Envelopes (prepared in advance by the project director).”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Kavanagh 2004, no separate results were reported for the AUDIT, Severity of Dependence Scale and the Drug Check, and results for number abstinent and number improved were collapsed, giving high risk of reporting bias.
“Selective reporting (reporting bias) High risk No separate results for AUDIT, Severity of Dependence Scale and the Drug Check.Results for number abstinent and number improved were collapsed.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Logan 2015, selective reporting was at unclear risk of bias.
“Selective reporting (reporting bias) Unclear risk No protocol available.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Miller 2003, allocation concealment was judged at unclear risk of selection bias.
“Allocation concealment (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Martino 2018, random sequence generation was at low risk of bias.
“Random sequence generation (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor McDevitt-Murphy 2014, random sequence generation was at unclear risk of bias.
“Random sequence generation (selection bias) Unclear risk Insufficient information to permit judgement.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningFor MATCH 1993, blinding of assessors was at unclear risk of bias.
“Blinding (performance bias and detection bias) Assessors Unclear risk No blinding, but most outcomes were physiological, also used to validate selfreports, and not likely to be influenced by lack of blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenFor Marsden 2006, selective reporting was at low risk of bias.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the study hypotheses.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Mastroleo 2010, allocation concealment was at unclear risk of bias.
“Allocation concealment (selection bias) Unclear risk No mention of allocation concealment.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataFor Miller 2003, allocation concealment was at unclear risk of bias.
“Allocation concealment (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningFor Martin 2008, blinding of patients and providers was at low risk of bias.
“Blinding (performance bias and detection bias) Patients and providers Low risk No blinding, but most outcomes were physiological and also used to validate self-reports, and not likely to be influenced by lack of blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Miller 2003, blinding of assessors was judged at high risk of detection bias.
“Blinding (performance bias and detection bias) Assessors High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenFor Marín-Navarrete 2017, blinding of patients and providers was at high risk of bias.
“Blinding (performance bias and detection bias) Patients and providers High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningFor McDevitt-Murphy 2014, blinding of assessors was at high risk of bias.
“Blinding (performance bias and detection bias) Assessors High risk Only self-reported outcomes.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataFor Marín-Navarrete 2017, incomplete outcome data was at low risk of bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk 96%, 92.5%, and 95% follow-up for post-treatment, 8 weeks, and 16 weeks, respectively.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningFor Mertens 2014, blinding of assessors was at high risk of bias.
“Blinding (performance bias and detection bias) Assessors High risk Research interviewers were blinded to randomisation status, but only self-reported outcomes were assessed.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Mastroleo 2010, incomplete outcome data was at low risk of bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk 16% attrition at 3 months.Balanced.No reasons stated.ITT analysis performed (imputed missing data).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningFor Martin 2008, selective reporting was at low risk of bias.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the study purposes.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor McCambridge 2008, blinding of patients and providers was at unclear risk of bias.
“Blinding (performance bias and detection bias) Patients and providers Unclear risk No blinding but bogus pipeline.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataFor McCambridge 2008, blinding of assessors was at low risk of bias.
“Blinding (performance bias and detection bias) Assessors Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Miller 2003, blinding of patients and providers was at unclear risk of bias.
“Blinding (performance bias and detection bias) Patients and providers Unclear risk No blinding but urine toxicology.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Marín-Navarrete 2017, allocation concealment was at low risk of bias.
“Allocation concealment (selection bias) Low risk Central (online clinical trial management software).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Martino 2018, blinding of patients and providers was at high risk of bias.
“Blinding (performance bias and detection bias) Patients and providers High risk Unblinded”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenFor Miller 2003, blinding of assessors was at low risk of bias.
“Blinding (performance bias and detection bias) Assessors Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataFor McDevitt-Murphy 2014, allocation concealment was at unclear risk of bias.
“Allocation concealment (selection bias) Unclear risk Insufficient information to permit judgement.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductreasoningFor Martino 2018, other bias was at low risk of bias.
“Other bias Low risk In addition to self-reported substance use, urine samples were collected at each assessment:”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataFor Mastroleo 2010, selective reporting was at low risk of bias.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the study purposes.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenFor Martino 2018, allocation concealment was at low risk of bias.
“Allocation concealment (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Marín-Navarrete 2017, other bias was at unclear risk of bias.
“Other bias Unclear risk No demographic information at baseline reported.No results on urine toxicology screens reported.No additional sources of bias appear to be present.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Morgenstern 2009, blinding of assessors was judged at high risk of detection bias.
“Blinding (performance bias and detection bias) Assessors High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Marín-Navarrete 2017, random sequence generation was at low risk of bias.
“Random sequence generation (selection bias) Low risk Computer-based urn randomisation procedure, stratified by gender and primary substance of use.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Monti 2016, selective reporting was judged at unclear risk of reporting bias.
“Selective reporting (reporting bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Marín-Navarrete 2017, selective reporting was at low risk of bias.
“Selective reporting (reporting bias) Low risk Pre-planned secondary endpoints were not reported.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Martin 2008, other bias was at unclear risk of bias.
“Other bias Unclear risk Urinalysis to validate self-report.The treatment group reported significantly more days of cannabis use in the previous 90 days than the control group.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataFor McCambridge 2008, selective reporting was at low risk of bias.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the stated hypotheses.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenFor Martino 2006, blinding of assessors was at low risk of bias.
“Blinding (performance bias and detection bias) Assessors Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Monti 2016, incomplete outcome data were judged at high risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataFor Martin 2008, allocation concealment was at low risk of bias.
“Allocation concealment (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataFor McCambridge 2008, allocation concealment was at low risk of bias.
“Allocation concealment (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataFor Mastroleo 2010, blinding of assessors was at unclear risk of bias.
“Blinding (performance bias and detection bias) Assessors Unclear risk It is not stated whether assessors were blinded.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Monti 2016, blinding of assessors was judged at unclear risk of detection bias.
“Blinding (performance bias and detection bias) Assessors Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor MATCH 1993, selective reporting was at unclear risk of bias.
“Selective reporting (reporting bias) Unclear risk Primary outcomes measures (PDA (percent days abstinent) and DDD (drinks per drinking day)) reported incompletely (only by graphs).Outcome for drinking consequences only reported in tables for 9-and 15-month follow-up.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Morgenstern 2009, incomplete outcome data were judged at low risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor McDevitt-Murphy 2014, other bias was at unclear risk of bias.
“Other bias Unclear risk No differences between groups at baseline, only non-physiological (self-reported) outcomes available, no definition of a primary outcome, no sample size calculation reported, no additional sources of bias appear to be present.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataFor McCambridge 2008, random sequence generation was at unclear risk of bias.
“Random sequence generation (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor McDevitt-Murphy 2014, incomplete outcome data was at low risk of bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk 94% and 93% reported follow-up at 6 weeks and 6 months, respectively, with no differences between groups.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Monti 2016, blinding of patients and providers was judged at unclear risk of performance/detection bias.
“Blinding (performance bias and detection bias) Patients and providers Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataFor Martino 2018, blinding of assessors was at unclear risk of bias.
“Blinding (performance bias and detection bias) Assessors Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataFor Martino 2018, selective reporting was at low risk of bias.
“Selective reporting (reporting bias) Low risk All primary outcome measures reported in the protocol were reported in the study.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningFor MATCH 1993, other bias was at low risk of bias.
“Other bias Low risk Collateral report, laboratory tests (blood and urine) as check on self-report.Breathalyser at each assessment point.Inclusion criteria contained no planned involvement for additional treatment during the study period.There were no differences between groups at baseline.No additional sources of bias appear to be present.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Miller 2003, blinding of patients and providers was judged at high risk of performance/detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Miller 2003, other bias was judged at unclear risk.
“Other bias Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Martin 2008, blinding of assessors was at low risk of bias.
“Blinding (performance bias and detection bias) Assessors Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Morgenstern 2009, allocation concealment was judged at unclear risk of selection bias.
“Allocation concealment (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenFor Mertens 2014, allocation concealment was at low risk of bias.
“Allocation concealment (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Miller 2003, random sequence generation was at low risk of bias.
“Random sequence generation (selection bias) Low risk Urn randomisation.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenFor Mastroleo 2010, other bias was at unclear risk of bias.
“Other bias Unclear risk Only self-reported outcomes.61/156 (39%) of randomised participants did not receive the intervention.Differences between groups at baseline were not reported.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductnone givenFor Martino 2006, selective reporting was at low risk of bias.
“Selective reporting (reporting bias) Low risk The published report included all expected outcomes based on the study purposes.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Monti 2016, allocation concealment was judged at unclear risk of selection bias.
“Allocation concealment (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor MATCH 1993, random sequence generation was at low risk of bias.
“Random sequence generation (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Miller 2003, selective reporting was judged at unclear risk of reporting bias.
“Selective reporting (reporting bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor McDevitt-Murphy 2014, blinding of patients and providers was at high risk of bias.
“Blinding (performance bias and detection bias) Patients and providers High risk No blinding of participants and personnel.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Morgenstern 2009, random sequence generation was judged at low risk of selection bias.
“Random sequence generation (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataFor Martino 2006, other bias was at high risk of bias.
“Other bias High risk Only self-reported outcomes.There were differences at baseline in alcohol composite score and legal involvement.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Marsden 2006, other bias was at low risk of bias.
“Other bias Low risk Stimulant toxicology testing on a random 30%.There were no differences between groups at baseline.No additional sources of bias appear to be present.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataFor Martino 2006, allocation concealment was at unclear risk of bias.
“Allocation concealment (selection bias) Unclear risk Insufficient information to permit judgement.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningFor McCambridge 2008, other bias was at low risk of bias.
“Other bias Low risk A bogus pipeline approach was used in addition to self-report.There were no differences between groups at baseline.No additional sources of bias appear to be present.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Martino 2006, random sequence generation was at low risk of bias.
“Random sequence generation (selection bias) Low risk Urn randomisation.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductnone givenFor Martino 2006, blinding of patients and providers was at low risk of bias.
“Blinding (performance bias and detection bias) Patients and providers Low risk Blinding of providers was not possible, but participants could have been blinded.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Miller 2003, random sequence generation was judged at low risk of selection bias.
“Random sequence generation (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataFor Martin 2008, random sequence generation was at low risk of bias.
“Random sequence generation (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Morgenstern 2009, blinding of patients and providers was judged at high risk of performance/detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Morgenstern 2009, selective reporting was judged at unclear risk of reporting bias.
“Selective reporting (reporting bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningFor MATCH 1993, allocation concealment was at unclear risk of bias.
“Allocation concealment (selection bias) Unclear risk Randomisation process was centrally controlled by the co-ordination centre.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Mertens 2014, random sequence generation was at unclear risk of bias.
“Random sequence generation (selection bias) Unclear risk Insufficient information provided.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Marín-Navarrete 2017, blinding of assessors was at low risk of bias.
“Blinding (performance bias and detection bias) Assessors Low risk Interview-based assessment of self-reported substance use:”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Monti 2016, other bias was judged at unclear risk.
“Other bias Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Martin 2008, incomplete outcome data was at low risk of bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk 20% were lost to follow-up.Equal attrition across groups.ITT analysis conducted.Reasons for attrition not reported.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenFor Martino 2018, incomplete outcome data was at low risk of bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor McDevitt-Murphy 2014, selective reporting was at unclear risk of bias.
“Selective reporting (reporting bias) Unclear risk No registration or protocol available.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFor Mastroleo 2010, random sequence generation was at unclear risk of bias.
“Random sequence generation (selection bias) Unclear risk No mention of allocation method.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Monti 2016, random sequence generation was judged at low risk of selection bias.
“Random sequence generation (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataFor Martino 2006, incomplete outcome data was at low risk of bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk 14% were lost to at least one follow-up, balanced across groups.Reasons for loss not stated.ITT analysis performed.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Miller 2003, incomplete outcome data were judged at unclear risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Saitz 2014, random sequence generation was judged at low risk of selection bias.
“Random sequence generation (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Parsons 2014, other bias was judged at unclear risk.
“Other bias Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Peterson 2006, allocation concealment was judged at unclear risk of selection bias.
“Allocation concealment (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Parsons 2009, allocation concealment was judged at unclear risk of selection bias.
“Allocation concealment (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Peterson 2006, blinding of assessors was judged at unclear risk of detection bias.
“Blinding (performance bias and detection bias) Assessors Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Rohsenow 2004, allocation concealment was judged at unclear risk of selection bias.
“Allocation concealment (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Morgenstern 2017, incomplete outcome data were judged at low risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Morgenstern 2012, incomplete outcome data were judged at low risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Morgenstern 2012, random sequence generation was judged at low risk of selection bias.
“Random sequence generation (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Peterson 2006, random sequence generation was judged at low risk of selection bias.
“Random sequence generation (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Parsons 2009, random sequence generation was judged at low risk of selection bias.
“Random sequence generation (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Murphy 2018, selective reporting was judged at low risk of reporting bias.
“Selective reporting (reporting bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Murphy 2010, blinding of patients and providers was judged at high risk of performance/detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Parsons 2014, selective reporting was judged at unclear risk of reporting bias.
“Selective reporting (reporting bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn Schaus 2009, other bias was judged at high risk.
“Other bias High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Schaus 2009, incomplete outcome data were judged at high risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Parsons 2014, blinding of assessors was judged at unclear risk of detection bias.
“Blinding (performance bias and detection bias) Assessors Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Morgenstern 2017, blinding of patients and providers was judged at high risk of performance/detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Murphy 2018, allocation concealment was judged at low risk of selection bias.
“Allocation concealment (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Rohsenow 2004, random sequence generation was judged at unclear risk of selection bias.
“Random sequence generation (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Saitz 2007, other bias was judged at unclear risk.
“Other bias Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Saitz 2007, incomplete outcome data were judged at low risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Murphy 2010, selective reporting was judged at high risk of reporting bias.
“Selective reporting (reporting bias) High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Murphy 2012, other bias was judged at unclear risk.
“Other bias Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Murphy 2010, other bias was judged at unclear risk.
“Other bias Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn Schaus 2009, selective reporting was judged at low risk of reporting bias.
“Selective reporting (reporting bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Saitz 2007, blinding of patients and providers was judged at high risk of performance/detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Morgenstern 2012, selective reporting was judged at unclear risk of reporting bias.
“Selective reporting (reporting bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Schaus 2009, blinding of patients and providers was judged at high risk of performance/detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn Logan 2015, people with heavier drinking were less likely than people with lighter drinking to be followed up, though no numbers were reported.
“Differences in response rates (people with heavier drinking were less likely than people with lighter drinking to follow-up), but no numbers were reported.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Murphy 2010, allocation concealment was judged at low risk of selection bias.
“Allocation concealment (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Murphy 2010, incomplete outcome data were judged at low risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn the included study assessed, other risk of bias was unclear because only non-physiological (self-reported) outcomes were available and there was no information on planned sample size or demographic baseline information per group.
“Other bias Unclear risk Only non-physiological (self-reported) outcomes available; no information on planned sample size or demographic baseline information per group.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Murphy 2018, other bias was judged at unclear risk.
“Other bias Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Morgenstern 2017, selective reporting was judged at unclear risk of reporting bias.
“Selective reporting (reporting bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Morgenstern 2012, blinding of patients and providers was judged at high risk of performance/detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Murphy 2012, blinding of patients and providers was judged at high risk of performance/detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Morgenstern 2012, allocation concealment was judged at unclear risk of selection bias.
“Allocation concealment (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Morgenstern 2017, blinding of assessors was judged at high risk of detection bias.
“Blinding (performance bias and detection bias) Assessors High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Saitz 2007, allocation concealment was judged at low risk of selection bias.
“Allocation concealment (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Morgenstern 2012, blinding of assessors was judged at high risk of detection bias.
“Blinding (performance bias and detection bias) Assessors High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Saitz 2007, selective reporting was judged at low risk of reporting bias.
“Selective reporting (reporting bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn Saitz 2014, other bias was judged at high risk.
“Other bias High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Saitz 2007, random sequence generation was judged at unclear risk of selection bias.
“Random sequence generation (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Morgenstern 2017, random sequence generation was judged at low risk of selection bias.
“Random sequence generation (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn Logan 2015, other risk of bias was unclear because only self-reported outcomes were used, no baseline values were reported, and no sample size calculation was reported.
“Other bias Unclear risk Only self-reported outcomes; no baseline values reported; no sample size calculation.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Murphy 2012, selective reporting was judged at unclear risk of reporting bias.
“Selective reporting (reporting bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Morgenstern 2009, other bias was judged at unclear risk.
“Other bias Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Rohsenow 2004, blinding of patients and providers was judged at unclear risk of performance/detection bias.
“Blinding (performance bias and detection bias) Patients and providers Unclear risk”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataIn the included study assessed, incomplete outcome data was at high risk of bias, with follow-up of 77% and 66% at 6 and 12 months and no information about causes for dropout or differences between groups.
“Incomplete outcome data (attrition bias) All outcomes High risk Follow-up of 77% and 66% at 6 and 12 months, with no information about causes for dropout and differences between groups.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Rohsenow 2004, incomplete outcome data were judged at unclear risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Morgenstern 2012, other bias was judged at unclear risk.
“Other bias Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Schaus 2009, random sequence generation was judged at unclear risk of selection bias.
“Random sequence generation (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Murphy 2012, random sequence generation was judged at low risk of selection bias.
“Random sequence generation (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Peterson 2006, blinding of patients and providers was judged at unclear risk of performance/detection bias.
“Blinding (performance bias and detection bias) Patients and providers Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Murphy 2018, blinding of patients and providers was judged at high risk of performance/detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Parsons 2009, blinding of patients and providers was judged at unclear risk of performance/detection bias.
“Blinding (performance bias and detection bias) Patients and providers Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Murphy 2018, blinding of assessors was judged at unclear risk of detection bias.
“Blinding (performance bias and detection bias) Assessors Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Parsons 2009, other bias was judged at unclear risk.
“Other bias Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Rohsenow 2004, selective reporting was judged at low risk of reporting bias.
“Selective reporting (reporting bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Saitz 2014, allocation concealment was judged at low risk of selection bias.
“Allocation concealment (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn Peterson 2006, selective reporting was judged at low risk of reporting bias.
“Selective reporting (reporting bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Murphy 2012, blinding of assessors was judged at high risk of detection bias.
“Blinding (performance bias and detection bias) Assessors High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Murphy 2012, allocation concealment was judged at unclear risk of selection bias.
“Allocation concealment (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn Saitz 2014, selective reporting was judged at low risk of reporting bias.
“Selective reporting (reporting bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Morgenstern 2017, allocation concealment was judged at unclear risk of selection bias.
“Allocation concealment (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn Saitz 2014, blinding of assessors was judged at low risk of detection bias.
“Blinding (performance bias and detection bias) Assessors Low risk”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductreasoningMost outcomes in the study concerned were physiological, were also used to validate self-reports, and were not likely to be influenced by lack of blinding.
“but most outcomes were physiological, also used to validate selfreports, and not likely to be influenced by lack of blinding.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Rohsenow 2004, other bias was judged at unclear risk.
“Other bias Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Saitz 2014, blinding of patients and providers was judged at unclear risk of performance/detection bias.
“Blinding (performance bias and detection bias) Patients and providers Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataIn the included study assessed, blinding of patients and providers was not possible, although study clinicians were blinded to patient randomisation prior to completion of the baseline assessment.
“Blinding (performance bias and detection bias) Patients and providers High risk Blinding not possible; study clinicians were blinded to patient randomisation prior to completion of the baseline assessment.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Murphy 2018, incomplete outcome data were judged at low risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Study design and conductown dataStudies were excluded from the review when quality conditions were not fulfilled, such as no coding, no recording, or no training described.
“Quality conditions not fulfilled: no coding, no recording, no training described.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Peterson 2006, other bias was judged at low risk.
“Other bias Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn Rohsenow 2004, blinding of assessors was judged at low risk of detection bias.
“Blinding (performance bias and detection bias) Assessors Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Saitz 2007, blinding of assessors was judged at unclear risk of detection bias.
“Blinding (performance bias and detection bias) Assessors Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Schaus 2009, blinding of assessors was judged at unclear risk of detection bias.
“Blinding (performance bias and detection bias) Assessors Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Murphy 2010, random sequence generation was judged at low risk of selection bias.
“Random sequence generation (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Schaus 2009, allocation concealment was judged at unclear risk of selection bias.
“Allocation concealment (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Parsons 2014, blinding of patients and providers was judged at high risk of performance/detection bias.
“Blinding (performance bias and detection bias) Patients and providers High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Parsons 2014, random sequence generation was judged at low risk of selection bias.
“Random sequence generation (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Morgenstern 2017, other bias was judged at unclear risk.
“Other bias Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Parsons 2014, allocation concealment was judged at unclear risk of selection bias.
“Allocation concealment (selection bias) Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Peterson 2006, incomplete outcome data were judged at unclear risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataStudies were excluded from the review when there was no fidelity check using video or audio.
“No fidelity check using video or audio.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Parsons 2014, incomplete outcome data were judged at high risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Murphy 2010, blinding of assessors was judged at high risk of detection bias.
“Blinding (performance bias and detection bias) Assessors High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Parsons 2009, selective reporting was judged at low risk of reporting bias.
“Selective reporting (reporting bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Parsons 2009, incomplete outcome data were judged at low risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Murphy 2018, random sequence generation was judged at low risk of selection bias.
“Random sequence generation (selection bias) Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn Saitz 2014, incomplete outcome data were judged at low risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes Low risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Parsons 2009, blinding of assessors was judged at unclear risk of detection bias.
“Blinding (performance bias and detection bias) Assessors Unclear risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Murphy 2012, incomplete outcome data were judged at high risk of attrition bias.
“Incomplete outcome data (attrition bias) All outcomes High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningSome of the searches in electronic databases are not up-to-date.
“Some of the searches in electronic databases are not up-to-date.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataPsychExtra and the International Bibliography of the Social Sciences were not searched in November 2010 because the authors did not have access.
“PsychExtra (search date 14 January 2008) and Cochrane Library Trusted evidence.Informed decisions.Better health.Cochrane Database of Systematic Reviews International Bibliography of the Social Sciences (November 2009) were not searched in November 2010 because we did not have access.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Study design and conductnone givenThe authors do not report fixed-effect meta-analyses because they believe there are systematic differences between the studies related to differences in interventions, populations, comparison groups, and outcome measures.
“We do not report fixed-effect meta-analyses because we believe that there are systematic differences between the studies, related to differences in interventions given, populations studied, comparison groups, and outcome measures.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductnone givenGoogle and Google Scholar were searched on 2 February 2009, and the authors did not believe that a new search was worthwhile in November 2010.
“Google and Google Scholar were searched on 2 February 2009, and we did not believe that a new search was worthwhile in November 2010.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Study design and conductreasoningThe authors did not do separate analyses for persons with and without mental problems.
“We did not do separate analyses for persons with and without mental problems.”
Quote in the paperSubstantial claim- Rests on an assumption: Mental problems are frequently co-occurring with substance use.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductnone givenC2 SPECTR and Bibliography of Nordic Criminology were searched on 23 November 2009, and these databases have not been updated since that date.
“C2 SPECTR and Bibliography of Nordic Criminology were searched on 23 November 2009, and these databases have not been updated since this date.”
Quote in the paperNot a substantial claim
The paper relies on this without support.
Publication bias poses a significant threat to the validity of any systematic review.
“Publication bias poses a significant threat to the validity of any systematic review.”
The paper relies on this without support.
In the very active field of motivational interviewing research, researchers are conducting many new studies that provide important insights into the effectiveness of this intervention.
“Second, in the very active field of motivational interviewing research, researchers are conducting many new studies that provide important insights into the effectiveness of this intervention.”
The paper relies on this without support.
Motivational interviewing and its quality criteria have evolved from its original development in 1983 to the present day.
“This is important because, as outlined above, motivational interviewing and its quality criteria have evolved from its original development in 1983 to the present day.”
The paper relies on this without support.
Substance-use diagnostic guidelines and classification systems are regularly updated.
“Third, substance-use diagnostic guidelines and classification systems are regularly updated.”
The paper relies on this without support.
Motivational interviewing is a widely-used approach which has generated a vast and ever-expanding field of research.
“This review is important because it provides a rigorous and upto-date evidence synthesis and meta-analysis of the effects of motivational interviewing, a widely-used approach which has generated a vast and ever-expanding field of research.”
The paper relies on this without support.
Different social contexts may influence substance-use patterns and the availability and accessibility of an intervention.
“as different social contexts may influence substance-use patterns and the availability and accessibility of an intervention.”
The paper relies on this without support.
Monitoring intervention fidelity is an important criterion to ensure that motivational interviewing adhered to Miller and Rollnick's principles and was delivered as intended.
“Monitoring intervention fidelity is an important criterion to ensure that motivational interviewing adhered to Miller and Rollnick's principles and was delivered as intended.”
The paper relies on this without support.
Non-blinding of physiological outcome assessment carries a lower risk of bias than non-blinding of non-physiological outcome assessment.
“Non-blinding of physiological outcome assessment carries a lower risk of bias than non-blinding of non-physiological outcome assessment.”
The paper relies on this without support.
Substance use outcomes in the included studies were self-reported.
“and substance use was self-reported.”
The paper relies on this without support.
The quality of a study may be high while the certainty of the evidence is susceptible to risk of bias.
“It is a particular methodological problem with this type of intervention because the quality of the study may be high while the certainty of the evidence is susceptible to risk of bias.”
The paper relies on this without support.
Mental problems are frequently co-occurring with substance use.
“mental problems are so frequently co-occurring with substance use”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
A Cochrane systematic review of 93 randomized controlled trials found that motivational interviewing (MI) led to a reduction in substance use post-intervention.
“A Cochrane systematic review analyzing 93 randomized controlled trials, involving 22,776 participants, revealed that MI led to a reduction in substance use post-intervention.”
From A Narrative Review of Current and Emerging Trends in the Treatment of Alcohol Use Disorder (2024) · cites this paper as [118]
The Discussion (Summary of main results) reports 91 RCTs and two quasi-RCTs involving 22,776 participants—not 93 RCTs. The Primary outcome section reports reduced substance use immediately after MI compared with no intervention, based on six studies, but a very small negative effect compared with treatment as usual. The unqualified post-intervention claim therefore overstates the review's findings. (LLM, conf=0.90)
Experimental — accuracy not yet measuredIn that review, MI demonstrated a standardized mean difference (SMD) of 0.48 compared to no intervention for substance use and an SMD of 0.26 for treatment retention.
“MI demonstrated a standardized mean difference (SMD) of 0.48 compared to no intervention, indicating a small to moderate effect, while also showing potential improvements in treatment retention, with an SMD of 0.26”
From A Narrative Review of Current and Emerging Trends in the Treatment of Alcohol Use Disorder (2024) · cites this paper as [118]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
The discussion overlooks a benefit versus usual treatment
MajorThe discussion says there was no benefit over treatment as usual at any follow-up, but the results report a positive medium-term effect whose confidence interval excludes zero.
“Compared to treatment as usual or any other active intervention, there was no benefit of motivational interviewing in terms of extent of substance use at any time during follow-up.”
“Medium-term follow-up: pooling nine studies with 1624 participants revealed a very small benefit of motivational interviewing (SMD 0.12, 95% CI 0.02 to 0.22; I 2 = 0%; low-certainty evidence; Analysis 2.1.3).”
D'Amico 2018 group sizes exceed the stated sample
MinorThe two intervention-group counts sum to 294, not the 249 participants stated for this study.
Reported 249 · recomputed 294
“Participants 249 youths in the USA who met criteria for at-risk substance use Interventions 1. CHAT intervention (brief MI, 15 to 20 min) (n = 153) 2. Usual care (n = 141)”
The reported maximum of nine sessions conflicts with an included study
MinorThe review states that included interventions had at most nine sessions, but its subgroup table lists Walitzer 2009 as having 12.
“The number of intervention sessions ranged from one to nine sessions, with one-third of studies (30) involving only one session.”
“Walitzer 2009 No Adults Alcohol 12 (60 min) NR”
Mastroleo 2010 group sizes nearly double the stated sample
MinorThe three listed group sizes total 238, whereas the study description says it had 122 participants.
Reported 122 · recomputed 238
“Participants 122 college students in the USA who met criteria for heavy drinking Interventions 1. Peer counselled MI with supervision (n = 74) 2. Peer counselled MI without supervision (n = 82) 3.No treatment control (n = 82)”
A low attrition-risk rating violates the review's stated cutoff
MinorThe review says a low-risk rating requires no more than 20% loss to follow-up. Ball 2007b is rated low despite 32% attrition at both reported follow-ups.
“We classified studies as having a low risk of bias in this domain if the number of participants lost to follow-up was clearly stated, the total number of participants lost to follow-up did not exceed 20%, and the difference between groups in terms of loss to follow-up did not exceed 20%.”
“Incomplete outcome data (attrition bias) All outcomes Low risk 32% attrition at 8 weeks after treatment.32% attrition at 16 weeks after treatment.”
The risk-of-bias domain count changes
MinorThe methods enumerate seven risk-of-bias domains, but the sensitivity-analysis description refers to all five domains.
“We assessed the following domains: randomisation procedure, allocation concealment, blinding of participants and providers, blinding of outcome assessors, incomplete outcome data, selective reporting, and other bias.”
“We assessed the impact of all five risk of bias domains independently.”
Cited works that were retracted
Works this paper cites that were later retracted, from the retraction notices publishers deposit. Major when the notice came out before this paper was published.
Cites a retracted work: 10.1016/j.jsat.2017.04.015
MajorThe cited work was retracted on 2017-04-23 (notice 10.1016/j.jsat.2017.04.015), before this paper was published (2023-12-12). Its authors could have known.
Cited work 10.1016/j.jsat.2017.04.015 · retracted 2017-04-23 · notice 10.1016/j.jsat.2017.04.015 · this paper published 2023-12-12
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A Narrative Review of Current and Emerging Trends in the Treatment of Alcohol Use Disorder
Celik, M., Gold, M. S., & Fuehrlein, B. (2024) · Brain Sciences · doi:10.3390/brainsci14030294 · Cited by 25 · see citing works
“MI demonstrated a standardized mean difference (SMD) of 0.48 compared to no intervention, indicating a small to moderate effect, while also showing potential improvements in treatment retention, with an SMD of 0.26 [118].”
MethodInfluentialBreaking barriers: addressing opioid stigma in chronic pain and opioid use disorder
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Pharmacists’ Contributions to the Management of Mental Health Conditions: A Comprehensive Review
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Düring, S. W., Sivertsen, D. M., & Johansen, K. S. (2025) · Journal of Dual Diagnosis · doi:10.1080/15504263.2025.2478900 · Cited by 6 · see citing works
“Further, they underline that the evidence is limited (Schwenker et al., 2023).”
Mordal, J., Juya, F., Holtan, L., Vederhus, J., Opheim, A., Brenna, I. H., Enger, A., Weimand, B. M., Solli, K. K., & Tanum, L. (2025) · Addiction Science & Clinical Practice · doi:10.1186/s13722-025-00576-9 · Cited by 6 · see citing works
“Nevertheless, addressing and resolving ambivalence has long been a key feature in substance use treatment, such as in motivational interviewing [32].”
When life gets complicated: Food allergy, food insecurity, mental health, and substance use disorder
Gupta, E., Conway, A. E., Kartha, N., Verdi, M., Madan, J. C., Anagnostou, A., Abrams, E. M., Greenhawt, M., White, A. A., Mustafa, S. S., et al. (2025) · Annals of Allergy Asthma & Immunology · doi:10.1016/j.anai.2025.05.030 · Cited by 5 · see citing works
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Outcomes and challenges of motivational interviewing in dual diagnosis treatment—A systematic review
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“Some existing reviews show no statistically significant difference when compared to routine care (Schwenker et al., 2023) (Hunt et al., 2019).”
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“Research conducted on patients with alcohol addiction, physical activity, and other conditions has revealed that motivational interviewing can enhance individuals’ psychological well-being and improve self-care abilities [19, 20].”
Wu, E. G., Chu, W., Miller, S. J., Moskal, M., Bodalski, E. A., Frary, S. G., & Harrison, S. E. (2025) · Community Mental Health Journal · doi:10.1007/s10597-025-01542-0 · Cited by 2 · see citing works
Kenya, S., Young, B., Escarfuller, S., et al. (2025) · PLoS ONE · doi:10.1371/journal.pone.0316300 · Cited by 1 · see citing works
“Historically, MI has been used by trained clinicians and counselors to support patients with substance use and addiction disorders [32,33].”
Moore, E., Vallejo, J. D., Sidell, M., Li, X., Delacroix, E., Young, D. R., Kunani, P., Resnicow, K., & Koebnick, C. (2025) · Patient Education and Counseling · doi:10.1016/j.pec.2025.109173 · Cited by 1 · see citing works
Sancho-Domingo, C., Garmy, P., & Norell‐Clarke, A. (2025) · International Journal of Addiction Nursing · doi:10.1097/jan.0000000000000651 · Cited by 1 · see citing works
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Hu, R., Yang, Y., Yang, Y., Kong, J., Luo, J., Yang, W., Chen, J., Liu, J., Zeng, H., Zhang, L., et al. (2026) · JMIR Formative Research · doi:10.2196/89077 · Cited by 1 · see citing works
“…counseling approach to facilitating behavior change [10], has been proven effective in promoting health behavior change across a variety of behaviors [11,12], such as smoking cessation [13], weight loss [14], substance use [15], physical activity [16,17], and chronic disease self-management [18].”
Nordeck, C. D., Sharma, A., Terplan, M., Dušek, K., Gilliams, E. A., & Gryczynski, J. (2023) · Journal of Psychiatry and Brain Science · doi:10.20900/jpbs.20230010 · Cited by 1 · see citing works
“Participants with untreated OUD are randomized to one of three arms: Usual Care (UC) enhanced with overdose prevention resources (i.e., naloxone), Patient Navigation (PN), or Patient Navigation + Buprenorphine Initiation (PN + BUP).”
MethodSinchi-Sinchi, H., Burgos‐Benavides, L., Ramírez, A., Rodríguez‐Díaz, F. J., & Díez, F. J. H. (2025) · Research Square · doi:10.21203/rs.3.rs-6824138/v1 · Cited by 1 · see citing works
Preda, A. (2014) · Cochrane Clinical Answers · doi:10.1002/cca.479
Dion, K.-M., Ferland, F., Farand, L., Gauvin, L. I., & Fleury, M. (2024) · Healthcare policy · doi:10.12927/hcpol.2024.27333
Kavirajan, H. (2024) · Cochrane Clinical Answers · doi:10.1002/cca.4448
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Motivational interviewing for alcohol use reduction in Thai patients
Muangnang, R., Singhasuriya, M., & Carvalho, A. A. D. S. (2025) · Open Medicine · doi:10.1515/med-2025-1307
“According to other authors [10], MI operates through the interaction of four fundamental processes: engaging, focusing, evoking, and planning.”
Friedmann, P. D., Friedmann, P. D., Ferguson, W. J., Bovell-Ammon, B. J., Stopka, T. J., & Evans, E. (2025) · Addiction Science & Clinical Practice · doi:10.1186/s13722-025-00641-3 · Cited by 1 · see citing works
“For example, motivational interviewing is used in both mental health [38] and substance use counseling [39].”
Neurologic Complications of Drug and Alcohol Use
Goss, A. (2026) · CONTINUUM Lifelong Learning in Neurology · doi:10.1212/cont.0000000000001676
Sleight, A. G., Weschler, S. B., Jones, J. M., Wood, K. C., Pergolotti, M., Williams, C., Brick, R. S., Lyon, S., Virani, A., Takata, S. C., et al. (2026) · Disability and Rehabilitation · doi:10.1080/09638288.2026.2613637
“Motivational interviewing is a common strategy employed by many different members of the healthcare team to support a patient through this challenging process [38]. in some cases, a referral to an addiction specialist is recommended.”
Koebnick, C., Sidell, M., Vallejo, J. D., Li, X., Delacroix, E., Young, D., Kunani, P., & Resnicow, K. (2026) · JMIR Research Protocols · doi:10.2196/78792
“Originally developed to treat substance use disorders [21], MI has since demonstrated efficacy across a range of health behaviors, including diet, physical activity, and weight management [16,22-24].”
Chung, A. K. K., Tang, S. W., Tse, C. Y., Dong, Y. D., Law, J. K. C., & Leung, W. (2026) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2026.1757627
“It therefore highlighted the critical need for developing a more comprehensive treatment plan involving other modalities, such as motivational interviewing and motivational enhancement therapy, to enhance the possibility of complete abstinence (46).”
Braun, A. C., Spees, C., Liebe, R. A., Corcoran, S., & Houck, J. M. (2026) · Health Education & Behavior · doi:10.1177/10901981261435543
Bell, J. S., Dewey, J. M., Watson, D. P., Johnstone, C., Palmer, J. S., Kurz, R., & Grella, C. E. (2026) · Addiction Science & Clinical Practice · doi:10.1186/s13722-026-00666-2
“Over the past several decades, engagement strategies have shifted towards motivational approaches that emphasize empathy, autonomy, and collaboration [20–22].”
Park, J. J., Zhang, K., Lee, G., Lee, M., Mohapatra, A., & Potenza, M. N. (2026) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2026.2665653
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Elsayed, M., Belisario, K. L., Blakely, A., Syan, S. K., Levitt, E., Garber, M. L., MacKillop, E., Balodis, I. M., Sweet, L. H., & MacKillop, J. M. (2026) · Alcohol and Alcoholism · doi:10.1093/alcalc/agag033
“This dynamic and adaptable approach has gained widespread recognition as a key inter vention in the treatment of alcohol use disorder (AUD) and other addictive behaviours ( Nyamathi et al. 2010, Miller and Rollnick 2013, Hurlocker et al. 2023, Schwenker et al. 2023).”
Motivational Interviewing and the 5A Model in Primary Care
Sönmez, T. G., & Fi̇dancı, İ. (2026) · Arşiv Kaynak Tarama Dergisi · doi:10.17827/aktd.1817154
Co-occurring Psychiatric Disorders
Maruti, S. (2026) · Springer eBooks · doi:10.1007/978-3-032-24174-0_22
Brazeau, B. W., Cunningham, J. A., & Hodgins, D. C. (2026) · International Gambling Studies · doi:10.1080/14459795.2026.2697447
Editorial: Emerging treatment approaches for substance use disorders
Garza, D. M., Blokhin, I. O., Brett, J., & Salloum, I. M. (2026) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2026.1926719
“Non-pharmacological interventions have also been employed to address SUDs, including cognitive behavioral therapy (CBT) (15), community reinforcement approach (16), motivational interviewing (17), and contingency management (18), with varying degrees of ef fi cacy.”
Wood, R. M., Thomson, P. M., & Creavin, S. (2026) · Health Care Management Science · doi:10.1007/s10729-026-09785-3
Innovative Suchtbehandlung im Maßregelvollzug
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Forray, A. (2026) · Current Addiction Reports · doi:10.1007/s40429-026-00775-7
“Importantly, adopting a harm reduction lens rather than an abstinence-only approach may help increase engagement among individuals who are not yet ready to fully cease alcohol use by supporting incremental behavior change and reducing barriers to participation [56].”
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ผลของโปรแกรมเสรมสรางแรงจงใจรวมกบการปรบความคดและพฤตกรรมตอความรวมมอในการรกษาดวยยาของผปวยโรคซมเศรา
อันอามาตย์, ล., โคตรสมบัติ, ช., & ปราบมะเริง, บ. (2026) · Journal of Mental Health of Thailand - วารสารสุขภาพจิต แห่งประเทศไทย · doi:10.64838/jmht.2026.289192
de Vries, M., Bol, E., van Yperen, M., Breeuwsma-Geurts, E., de Beurs, E., & Goudriaan, A. (2024) · Gedragstherapie. · doi:10.5553/tg/016774542024057004011
- Authors
- Schwenker, R., Dietrich, C. E., Hirpa, S., Nothacker, M., Smedslund, G., Frese, T., & Unverzagt, S.
- Affiliations
- Martin Luther University Halle-Wittenberg (DE)
- Institute of General Practice and Family Medicine; Center of Health Sciences, Martin Luther University Halle Wittenberg; Halle (Saale) Germany
- Philipps University of Marburg (DE)
- Norwegian Institute of Public Health (NO)
- Venue
- Cochrane Database of Systematic Reviews
- Publisher
- Wiley
- Published
- 2023-12-12
- Volume
- 2023
- Issue
- 12
- Pages
- CD008063-CD008063
- ISSN
- 1361-6137 (ISSN-L)
- 1465-1858
- PMC
- PMC10714668
- OpenAlex
- W4389607915
- Cited by
- 56
- References
- 415
- Citations by year
- 2026: 25 · 2025: 20 · 2024: 9 · 2023: 1 · 2014: 1
- FWCI
- 2.14
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Cochrane Database of Systematic Reviews (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Epidemiology › Substance Abuse Treatment and Outcomes
- Social Sciences › Psychology › Applied Psychology › Behavioral Health and Interventions
- Social Sciences › Psychology › Clinical Psychology › Psychotherapy Techniques and Applications
- Keywords
- motivational interviewing, motivational enhancement therapy, substance use reduction, substance use disorders, alcohol consumption, drug use, readiness to change, treatment retention, ambivalence, treatment effectiveness, long-term outcomes, relapse prevention, treatment cost-effectiveness, treatment acceptability
- MeSH terms
- Affect, Humans, Motivation, Time Factors, Substance-Related Disorders, Motivational Interviewing
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